Maria I. New, M.D.
Publications
1. New MI, McNamara H, Kretchmer N:
Accumulation of para‑amino‑hippurate by slices of kidney from
rabbits of various ages. Proc Soc Exp
Biol Med 102:558‑560, 1959.
2. New MI, Roberts TN, Bierman EL, Reader
GG: The significance of blood lipid alterations in diabetes mellitus. Diabetes 12:208‑212, 1963.
3. New MI: Endocrine factors in
growth. Medical Science 15:52‑55,
1964.
4. Bauer CH, New MI, Miller JM:
Cerebrospinal fluid protein values of premature infants. J Pediatr 6:1017‑1022, 1965.
5. New MI, Miller B, Peterson RE:
Aldosterone excretion in normal children and in children with adrenal
hyperplasia. J Clin Invest 45:412‑428,1966.
6. New MI, Peterson RE: Disorders of
aldosterone secretion in childhood. Pediatr
Clin North Am 13:43‑58, 1966.
7. Greenberg AJ, Arboit JM, New MI,
Worthen HG: Normotensive secondary hyperaldosteronism. J Pediatr 69:719‑727, 1966.
8. Bongiovanni AM, Eberlein WR,
9. New MI, Peterson RE: A new form of congenital
adrenal hyperplasia. J Clin
Endocrinol Metab 27:300‑305, 1967.
10. Grossman H, New MI: Precocious sexual
development: Roentgenographic aspects. Am
J Roent Rad Ther Nucl Med 100:48‑62, 1967.
11. Nadler AC, Sonenberg M, New MI,
12. Curi JFJ, Vanucci RC, Grossman H, New MI:
Elevated serum gonadotropins in Silver's syndrome. Am J Dis Child 114:658‑661,
1967.
13. New MI, Peterson RE: Aldosterone in
childhood, In Advances in Pediatrics, SZ Levine (ed). Year Book Medical Publishers, Chicago, 15:111‑136,
1968.
14. New MI, Gross JM, Peterson RE: Double
isotope dilution derivative technique for testosterone glucuronoside in
urine. Acta Endocrinologica 58:77‑97,
1968.
15. New MI: Congenital adrenal hyperplasia. Pediatric Clinics of
16. New MI, Seaman MP, Peterson RE: A method
for the simultaneous determination of the secretion rates of cortisol, 11‑desoxycortisol,corticosterone, 11‑desoxycorticosterone
and aldosterone. J Clin Endocrinol
Metab 29:514‑522, 1969.
17. Merkatz IR, New MI, Peterson RE, Seaman
MP: Prenatal diagnosis of adrenogenital syndrome by amniocentesis. J Pediatr 75:977‑982, 1969.
18. Simpson JL, Allen Jr FH, New MI, German
J: Absence of close linkage between the locus for Xg and the locus for
anhidrotic ectodermal dysplasia. Vox
Sang 17:465‑467, 1969.
19. New MI: Antenatal diagnosis of the adrenogenital
syndrome (Letter to the Editor). Lancet 1:83, 1970.
20. New MI, Seaman MP: Secretion rates of
cortisol and aldosterone precursors in various forms of congenital adrenal
hyperplasia. J Clin Endocrinol Metab 30:361‑371, 1970.
21. New MI (with the technical assistance of
Suvannakul L): Male pseudohermaphroditism due to 17a‑hydroxylase
deficiency. J Clin Invest 49:1930‑1941,
1970.
22. New MI: Endocrinological disorders. Bull Sloane Hosp Women 16:91‑99,
1970.
23. New MI: Methods for the diagnosis of
congenital adrenal hyperplasia. In: FW
Sunderman and FW Sunderman (eds), Laboratory Diagnosis of Endocrine
Diseases. Warren H Green Inc, St
Louis, 1971, pp 517-524.
24. Morillo‑Cucci G, New MI, Simpson
JL, Allen Jr FH, German J: Abnormalities of human sex chromosomes III
Duplication in the long arm of the Y chromosome (45,X/46,XYq+) in Y‑gonadal
dysgenesis. Ann Genet 14:113‑120,
1971.
25. Levine LS, New MI: Preoperative detection
of hidden testes, Am J Dis Child 121:176‑178, 1971.
26. Bullock LP, New MI: Testosterone and
cortisol concentration in spermatic, adrenal and systemic venous blood in adult
male guinea pigs. Endocrinology 88:523‑526, 1971.
27. Simpson JL, New MI, Peterson RE, German
J: Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs. In: Proceedings of
the Third Conference on Clinical Delineation of Birth Defects, VA McKusick
(ed), In: Birth Defects: Original Article Series, vol 7, 1971, pp 140‑144.
28. New MI, Parks GA, Landey S, Wiedemann E:
Dwarfism associated with defective sulfation factor generation, Clin Res 19:378, 1971.
29. Parks GA, Bermudez JA, Anast CS,
Bongiovanni AM, New MI: Pubertal boy with the 3ß‑hydroxysteroid
dehydrogenase defect. J Clin
Endocrinol Metab 33:269‑278, 1971.
30. Giombetti R, Hagstrom JWC, Landey S.
Young MC, New MI: Cushing's syndrome in infancy: a case complicated by monilial
endocarditis. Am J Dis Child 122:264‑266, 1971.
31. Zachmann M, Vollmin JA, New MI, Curtius H‑CH,
Prader A: Congenital adrenal hyperplasia due to deficiency of 11ß‑hydroxylation
of 17a‑hydroxylated steroids. J
Clin Endocrinol Metab 33:501‑508, 1971.
32. Sonenberg M, Yamasaki N, Kikutani M,
Swislocki NI, Levine LS, New MI: Studies on active fragments of bovine growth
hormone. In: A Pecile and EE Muller (eds), Growth and Growth Hormone,
In: Excerpta Medica International Congress Series, No 244. 1972, pp
75-90.
33.
34. New MI, Schwartz E, Parks GA, Landey S,
Wiedemann E: Pseudohypopituitary dwarfism with normal plasma growth hormone and
low serum sulfation factor. J Pediatr 80:620‑626, 1972.
35. Levine LS, New MI, Pitt P, Peterson RE:
Androgen production in boys with sexual precocity and congenital adrenal
hyperplasia. Metabolism 21:457‑464
1972.
36. Shanies DD, Hirschhorn K, New MI:
Metabolism of testosterone‑14C by cultured human cells. J Clin Invest 51:1459‑1468,
1972.
37. New MI: Adrenogenital syndrome. In: A Dorfman (ed), Antenatal Diagnosis,
A University of Chicago Press, Chicago, 1972, pp 153‑160.
38. Opitz JM, Simpson JL, Sarto GE, Summitt
RL, New MI, German J: Pseudovaginal perineoscrotal hypospadias. Clin Genet 3:1‑26, 1971.
39. New MI: Ambiguous genitalia. Ortho Panel, 16:2‑5, 1973.
40. Dahms WT, Gray G, Vrana M, New MI:
Adrenocortical adenoma and ganglioneuroblastoma in a child: A case presenting
as Cushing syndrome with virilization. Am
J Dis Child 125:608‑611, 1973.
41. New MI, Siegal EJ, Peterson RE:
Dexamethasone‑suppressible hyperaldosteronism. J Clin Endocrinol
Metab 37:93‑100, 1973.
42. New MI,
Levine LS: Congenital adrenal hyperplasia. In: H Harris and K Hirschhorn (eds), Advances
in Human Genetics, vol 4, Plenum Press,
43. Levine LS, Sonenberg M, New MI: Metabolic
effects in children of a 37 amino acid fragment of bovine growth hormone. J Clin Endocrinol Metab 37:607‑615,
1973.
44. Saenger P, Shanies DD, New MI: Influence
of medroxyprogesteroneacetate on testosterone metabolism by cultured human
fibroblasts: A model for drug steroid interaction. J Clin Endocrinol Metab 37:760‑764,
1973.
45. McCrory WW, New MI, Yaffe SJ: Drugs and the
Unborn Child, sponsored by The National Foundation‑March of Dimes, March,
1973. Clin Pharmacol Therap 14(2), 1973.
46. Sonenberg M, Levine LS, New MI, Saxena
BB: Fragments of growth hormone, In:
47. Parks GA, Dumars KW,
48. Saenger P, Wiedemann E, Schwartz E, Korth‑Schutz
S, Lewy JE, Riggio RR, Rubin AL, Stenzel KH, New MI: Somatomedin and growth
after renal transplantation, Pediatr Res 8:163‑169, 1974.
49. Korth‑Schutz S, Levine LS, Merkatz
IR, New MI: An unusual case of Cushing's syndrome, Hilus cell tumor and
polycystic ovaries. J Clin Endocrinol
Metab 38:794‑800, 1974.
50. Bennett SP, Levine LS, Siegal EJ, Lewy
JE, Susin M, Peterson RE, New MI: Juvenile hypertension caused by
overproduction of renin with in a renal segment. J Pediatr 84:689‑695, 1974.
51. Saenger P, Levine LS, Wiedemann E,
Schwartz E, New MI: Growth with absent growth hormone by radioimmunoassay
(Letter to the Editor). J Pediatr 85:137‑138, 1974.
52. Parks GA, Korth‑Schutz S, Penny R,
Hilding RF, Dumars KW,
53. Canale VC, Steinherz P, New MI, Erlandson
M: Endocrine function in thalassemia major. Ann NY Acad Sci 232:333‑345, 1974.
54. New MI,
Levine LS: Congenital adrenal hyperplasia. Ped
Annals 3:27‑53, 1974.
55. Rifkind AB, Bennett S, Forster ES, New
MI: Components of the heme biosynthetic pathway and mixed function oxidase
activity in human fetal tissues. Biochem
Pharmacol 24:839‑846, 1975.
56. Lewy JE, New MI: Growth in children with
renal failure. Am J Med 58:65‑68,
1975.
57. Doberne Y, Levine LS, New MI: Elevated
urinary testosterone and androstenediol in precocious adrenarche. Pediatr Res 9:794‑797, 1975.
58. Saenger P,
59. Saenger P, Schwartz E, Wiedemann E,
Levine LS, Tsai M, New MI: The interaction of growth hormone, somatomedin and oestrogen
in patients with Turner's syndrome. Acta
Endocrinologica 81:9‑18, 1976.
60. Levine LS, Lewy JE, New MI: Hypertension
in high school students: Evaluation in
61. Korth‑Schutz S, Levine LS, New MI
(with the technical assistance of DM Chow), Serum androgens in normal
prepubertal and pubertal children and in children with precocious
adrenarche. J Clin Endocrinol Metab 42:117‑124, 1976.
62. Doberne Y, New MI: Urinary androstanediol
and testosterone in adults. J Clin
Endocrinol Metab 42:152‑154, 1976.
63. Saenger P, Levine LS, Wiedemann E,
Schwartz E, New MI: Somatomedin in cerebral gigantism (Letter to the
Editor). J Pediatr 88:155‑156,
1976.
64. New MI, Baum CJ, Levine LS: Nomograms
relating aldosterone excretion to urinary sodium and potassium in the pediatric
population: Their application to the study of childhood hypertension. Am J Cardiol 37:658‑666, 1976.
65. Korth‑Schutz S, Levine LS, New MI
(with the technical assistance of DM Chow), Evidence for the adrenal source of
androgens in precocious adrenarche. Acta
Endocrinologica 82:342‑352, 1976.
66. Korth‑Schutz S, Levine LS, New MI
(with the technical assistance of DM Chow): Dehydroepiandrosterone sulfate (DS)
levels, a rapid test for abnormal adrenal androgen secretion. J Clin Endocrinol Metab 42:1005‑1013,1976.
67. Wachtel SS, Koo GC, Breg WR, Thaler HT,
Dillard GM, Rosenthal IM, Dosik H, Gerald PS, Saenger P, New MI, Lieber E,
Miller OJ: Serologic detection of a Y‑linked gene in XX males and XX true
hermaphrodites. New Engl J Med 295:750‑754, 1976.
68. Saenger P, Levine LS, Wachtel SS, Korth‑Schutz
S. Doberne Y, Koo GC, Lavengood Jr RW, German III JL, New MI: Presence of H‑Y
antigen and testis in 46,XX true hermaphroditism, evidence for Y‑chromosomal
function, J Clin Endocrinol Metab 43:1234‑1239, 1976.
69. New MI, Peterson RE, Saenger P, Levine
LS: Evidence for an unidentified ACTH‑induced steroid hormone causing
hypertension. J Clin Endocrinol Metab 43:1283‑1293, 1976.
70. New MI: Prenatal diagnosis of congenital
adrenal hyperplasia, In: MI New, RH Fiser Jr (eds), Diabetes and Other
Endocrine Disorders During Pregnancy and in the Newborn, In: Progress in
Clinical and Biological Research, vol 10, Alan R Liss, New York, 1976, pp
205‑219.
71. Rifkind AB, Canale V, New MI: Antipyrine
clearance in homozygous ß‑thalassemia. Clin Pharm Therap 20:476‑483, 1976.
72. Korth‑Schutz S, Levine LS, Roth JA,
Saenger P, New MI: Virilizing adrenal tumor in a child suppressed with
dexamethasone for three years: Effect of o,p'‑DDD on serum and urinary
androgens. J Clin Endocrinol Metab 44:433‑439, 1977.
73. New MI: Present status of prenatal
diagnosis of congenital adrenal hyperplasia, In: PA Lee, LP Plotnick, AA
Kowarski and CJ Migeon (eds), Congenital Adrenal Hyperplasia, University
Park Press,
74. Levine LS, Korth‑Schutz S, Saenger
P, Sweeney III WJ, Beling CG, New MI: Disordered puberty in treated congenital
adrenal hyperplasia. In: PA Lee, LP
Plotnick, AA Kowarski and CJ Migeon (eds), Congenital Adrenal Hyperplasia, University Park Press, Baltimore, 1977, pp 361‑378.
75. Ulick S, Ramirez LC, New MI: An
abnormality in steroid reductive metabolism in a hypertensive syndrome. J Clin Endocrinol Metab 44:799‑802,
1977.
76. New MI, Levine LS, Biglieri EG, Pareira
J, Ulick S: Evidence for an unidentified steroid in a child with apparent
mineralocorticoid hypertension. J
Clin Endocrinol Metab 44:924‑933, 1977.
77. New MI, Levine LS: Mineralocorticoid
hypertension in childhood. Mayo Clin
Proc 52:323‑328, 1977.
78. Koo GC, Wachtel SS, Saenger P, New MI,
Dosik H, Amarose AP, Dorus E, Ventruto V: H‑Y antigen: Expression in
human subjects with the testicular feminization syndrome. Science 196:655‑656, 1977.
79. New MI, Levine LS: An unidentified ACTH‑stimulable adrenal
steroid in childhood hypertension. In:
MI New and LS Levine (eds), Juvenile Hypertension, Raven Press,
80. New MI: Prenatal diagnosis of congenital
adrenal hyperplasia. In: HL Vallet and
IH Porter (eds), Genetic Mechanisms of Sexual Development, Academic
Press,
81. Saenger P, Goldman AS, Levine LS, Korth‑Schutz
S, Muecke EC, Katsumata M, Doberne Y, New MI: Prepubertal diagnosis of steroid
5a‑reductase deficiency. J Clin
Endocrinol Metab 46:627‑634, 1978.
82. Rosler A, Levine LS, Schneider B,
Novogroder M, New MI: The interrelationship of sodium balance, plasma renin
activity and ACTH in congenital adrenal hyperplasia. J Clin Endocrinol Metab 45:500‑512,
1977.
83. Saenger P, New MI: Inhibitory action of
dehydroepiandrosterone (DHEA) in fibroblast growth. Experientia 33:966‑967, 1977.
84. Saenger P, Levine LS, Wiedemann E,
Schwartz E, Korth‑Schutz S, Pareira J, Heinig B and New MI: Somatomedin
and growth hormone in psychosocial dwarfism. Padiatrie und Padologie (suppl 5):1‑12, 1977.
85. New MI,
Virdis R, Virdis P: Ipertensione ormonale dell'infanzia, Problemi Attuali in
Pediatria, 13‑26, 1977.
86. McVie R, Levine LS, New MI: The biologic
significance of the aldosterone concentration in saliva. Pediatr Res 13:755‑759, 1979.
87. Korth‑Schutz S, Virdis R, Saenger
P, Chow DM, Levine LS, New MI: Serum androgens as a continuing index of
adequacy of treatment of congenital adrenal hyperplasia. J Clin Endocrinol Metab 46:452‑458,
1978.
88. Pang S, Hotchkiss J, Drash AL, Levine LS,
New MI: Microfilter paper method for 17a‑hydroxyprogesterone
radioimmunoassay: Its application for rapid screening for congenital adrenal
hyperplasia. J Clin Endocrinol Metab 45:1003‑1008, 1977.
89. New MI, Rauh W: Childhood obesity and
hypertension. In: E Cacciari, Z Laron,
and S Raiti (eds), Obesity in Childhood, Proceedings of the Serono
Symposia, vol 17, Academic Press,
London, 1978, pp 87‑90.
90. Virdis R, Saenger P, Senior B, New MI:
Endocrine studies in a pubertal male pseudohermaphrodite with 17‑ketosteroid
reductase deficiency. Acta
Endocrinologica 87:212‑224, 1978.
91. New MI et al: Report of the Hypertension
Task Force: Current Research and Recommendations from the Task Force Subgroups
on Pediatrics and Genetics, Volume 6, DHEW Publication No (NIH) 79‑1628,
1979.
92. New MI: H‑Y antigen and abnormal
sex determination. In: OP Ghai (ed), New Developments in Pediatric Research, Proceedings of the XV International Congress of Pediatrics, Interprint, 1977,
pp 1119‑1120.
93. New MI, Levine LS: Pathogenesis and
endocrinological aspects of hypertension, In: OP Ghai (ed), New Developments
in Pediatric Research, Proceedings of the XV International Congress of
Pediatrics, Interprint, 1977, pp 61‑669.
94. New MI, Levine LS: Adrenocortical
hypertension. Pediatr Clin North Am 25:67‑81,
1978.
95. New MI: Ambiguous sex in the newborn:
Genital anomalies. In: Perspectives
on Sex and Gender‑A Multidisciplinary Conference, Institute for Urban
and Minority Education,
96. New MI, Levine LS: An unidentified ACTH
stimulable adrenal steroid in childhood hypertension. In: G Chiumello and Z Laron (eds), Recent
Progress in Pediatric Endocrinology, Proceedings of the Serono Symposia,
vol 12, Academic Press, New York, 1977.
pp 249‑267.
97. Oberfield SE, Levine LS, Carey RM, Bejar
R, New MI: Pseudohypoaldosteronism: Multiple target organ unresponsiveness to
mineralocorticoid hormones. J Clin
Endocrinol Metab 48:228‑234, 1979.
98. Ferraris J, Saenger P, Levine LS, New MI,
Pang S, Saxena BB, Lewy JE: Delayed puberty in males with chronic renal
failure. Kidney Int 18:344‑350,
1980.
99. New MI, Rauh W: Childhood obesity and hypertension. In: PJ Collipp (ed), Childhood Obesity,
2nd edition, PSG Publishing Co, Mass, 1980, pp 57‑61.
100. Rauh W, Levine LS, Gottesdiener K, New MI,
Mineralocorticoids, salt balance and blood pressure after prolonged ACTH
administration in juvenile hypertension. Klin Wochenschr, 56(suppl I):161‑167, 1978.
101. Levine LS, Novogroder M, Saxena B, Saenger
P, Saito I, New MI: Primary intracranial HCG‑producing germinoma in a boy
with congenital adrenal hyperplasia. Acta
Endocrinol 88:122‑131, 1978.
102. Levine LS, Zachmann M, New MI, Prader A,
Pollack MS, O'Neill GJ, Yang SY, Oberfield SE, Dupont B: Genetic mapping of the
21‑hydroxylase‑deficiency gene within the HLA linkage group. N Engl J Med 299:911‑915, 1978.
103. New MI: Guidelines for screening and
treating hypertensive children. Modern
Med 46:36‑45, 1978.
104. Pang S, Levine LS, Chow D, Sagiani F,
Saenger P, New MI: Dihydrotestosterone and its relationship to testosterone in
infancy and childhood. J Clin
Endocrinol Metab 48:821‑826, 1979.
105. Pang S, Levine LS, Chow DM, Faiman C, New
MI: Serum androgen concentrations in neonates and young infants with congenital
adrenal hyperplasia due to 21‑hydroxylase deficiency. Clin Endocrinol 11:575‑584,
1979.
106. Rauh W, Gottesdiener K, Chow D, Forster E,
Saenger P, Levine LS, New MI: Aldosterone response to prolonged ACTH infusion
in juvenile hypertension. Pediatr Res 14:1035‑39,1980.
107. Voccia E, Saenger P, Peterson RE, Rauh W,
Gottesdiener K, Levine LS, New MI: 6-Beta- hydroxycortisol excretion in
hypercortisolemic states. J Clin
Endocrinol Metab 48:467‑71,1979.
108. Lorenzen F, Pang S, New MI, Dupont B,
Pollack M, Chow DM, Levine LS: Hormonal phenotype and HLA‑genotype in
families of patients with congenital adrenal hyperplasia (21‑hydroxylase
deficiency). Pediatr Res 13:1356‑1360,
1979.
109. Rauh W, Levine LS, Gottesdiener K, Chow D,
Oberfield SE, Gunczler P, Pareira P, New MI: Adrenocortical function,
electrolyte metabolism, and blood pressure during prolonged adrenocorticotropin
infusion in juvenile hypertension. J
Clin Endocrinol Metab 49:52‑7, 1979.
110. New MI, Lorenzen F, Pang S, Gunczler P,
Dupont B, Levine LS: "Acquired" adrenal hyperplasia with 21‑hydroxylase
deficiency is not the same genetic disorder as congenital adrenal hyperplasia. J Clin Endocrinol Metab 48:356‑359,
1979.
111. Loggie JMH, New MI, Robson AM: Hypertension
in the pediatric patient: A reappraisal. J Pediatr 94:685‑699, 1979.
112. Loggie JMH, Londe S, New MI: Pediatric hypertension:
Add HBP to your list of childhood ills. Patient
Care 12:16‑24, 1978.
113. New MI, Gurpide E, Levine LS, Segal SJ,
Soyka LF, VanWyk JJ, Yaffe SJ: Report of the Conference on Estrogen Treatment
of the Young. Pediatrics 62 part
2 (suppl):1087‑1217, 1978.
114. Saenger P, Levine LS, Pang S, New MI:
Sexual ambiguity at birth. In: SJ Kogan and ESE Hafez (eds), Diagnosis in
Andrology, Vol 4, Martinus Nijhoff Publishers, Boston, 1980, pp 31‑52.
115. Yang SY, Levine LS, Zachmann M, New MI,
Prader A, Oberfield SE, O'Neill GJ, Pollack MS and Dupont B: Mapping of the 21‑hydroxylase
deficiency gene within the HLA linkage group. Transplant Proc 10:753‑755, 1978.
116. Brautbar C, Rosler A, Landau H, Cohen I,
Nelken D, Cohen T, Levine C, Sack J, Benderli A, Moses A, Lieberman E, Dupont
B, Levine LS and New MI: No linkage between HLA and congenital adrenal
hyperplasia due to 11‑ß‑hydroxylase deficiency (Letter to the
Editor). N Engl J Med 300:205‑206, 1979.
118. Oberfield SE, Case DB, Levine LS, Rapaport R,
Rauh W, New MI: Use of the oral angiotensin I‑converting enzyme inhibitor
(Captopril) in childhood malignant hypertension. J Pediatr 95:641‑644, 1979.
119. Pang S, Shine S, Levine LS and New MI:
Practical advances in cortisol and dehydroepiandrosterone sulfate
radioimmunoassay using microfilter paper method. J Lab Clin Med 95:515‑524, 1980.
120. Ulick S, Levine LS, Gunczler P, Zanconato
G, Ramirez LC, Rauh W, Rosler A, Bradlow HL, New MI: A syndrome of apparent
mineralocorticoid excess associated with defects in the peripheral metabolism
of cortisol. J Clin Endocrinol Metab 49:757‑764, 1979.
121. Saenger P, Schwartz E, Markenson AL,
Graziano JH, Levine LS, New MI, Hilgartner MW: Depressed serum somatomedin
activity in ß‑thalassemia. J
Pediatr 96:214‑218, 1980.
122. Pollack MS, Levine LS, Pang S, Owen RP,
Nitowsky HM, Maurer D, New MI, Duchon M, Merkatz IR, Sachs G, Dupont B:
Prenatal diagnosis of congenital adrenal hyperplasia (21‑hydroxylase
deficiency) by HLA typing. Lancet 1:1107‑8, 1979.
123. Pollack MS, Maurer D, Levine LS, New MI,
Pang S, Duchon MA, Owens RP, Merkatz IR, Nitowsky HM, Sachs G, Dupont B: HLA
typing of amniotic cells: The prenatal diagnosis of congenital adrenal
hyperplasia (21‑OH‑deficiency type). Transplant Proc XI:1726‑1728,
1979.
124. Newman CB, Levine LS, New MI: Endocrine
function in children with intrasellar and suprasellar neoplasms before and
after therapy. Am J Dis Child 135:259‑262, 1981.
125. New MI, Levine LS: Endocrine diseases. In:
E Wasserman and DS Gromish (eds), Survey of Clinical Pediatrics, 7th
edition, McGraw‑Hill Book Company,
126. Oberfield SE, Levine LS, Wellner D,
Novogroder M, Laino P, New MI: Ascorbic acid treatment in nephropathic cystinosis
in identical twins. Dev Pharmacol
Therap 2:80‑90, 1981.
127. Levine LS, New MI: Endocrine aspects of
hypertension. In: CGD Brook (ed), Clinical
Paediatric Endocrinology, Blackwell Scientific Publications,
128. O'Neill GJ, Pollack MS, Yang SY, Levine LS,
New MI, Dupont B: Gene frequencies and genetic linkage disequilibrium for the
HLA linked genes Bf, C2, C4S, C4F, 21‑hydroxylase deficiency and
glyoxalase I. Trans Proc 11:1713‑1718,
1979.
129. Lan NC, Matulich DT, Stockigt JR, Biglieri
EG, New MI, Winter JS, McKenzie JK, Baxter JD: Radioreceptor assay of plasma
mineralocorticoid activity: role of aldosterone, cortisol and
deoxycorticosterone in various mineralocorticoid‑excess states. Circ Res 46(suppl I):94‑100,
1980.
130. Mininberg DT, Levine LS, New MI: Current
concepts in congenital adrenal hyperplasia. Invest Urol 17:169‑175, 1979.
131. Lorenzen F, Pang S, New MI, Pollack MS,
Oberfield SE, Dupont B, Chow D, Schneider B, Levine LS: Studies of the C‑21
and C‑19 steroids and HLA genotyping in siblings and parents of patients
with congenital adrenal hyperplasia due to 21‑hydroxylase
deficiency. J Clin Endocrinol Metab 50:572‑577, 1980.
132. Levine LS, Rauh W, Gottesdiener K, Chow D,
Gunczler P, Rapaport R, Pang S, Schneider B, New MI: New studies of the 11ß‑hydroxylase
and 18‑hydroxylase enzymes in the hypertensive form of congenital adrenal
hyperplasia. J Clin Endocrinol Metab 50:258‑263, 1980.
133. Pang S, Levine LS, Cederqvist LL, Fuentes
M, Riccardi VM, Holcombe JH, Nitowsky HM, Sachs G, Anderson CE, Duchon MA,
Owens R, Merkatz I, New MI: Amniotic fluid concentrations of _5 and _4 steroids
in fetuses with congenital adrenal hyperplasia due to 21‑hydroxylase
deficiency and in anencephalic fetuses, J Clin Endocrinol Metab 51:223‑229,1980.
134. Pang S, Levine LS, Lorenzen F, Chow D,
Pollack MS, Dupont B, Genel M, New MI: Hormonal studies in obligate
heterozygotes and siblings of patients with 11ß‑hydroxylase deficiency
congenital adrenal hyperplasia. J
Clin Endocrinol Metab 50:586‑589, 1980.
135. Laron Z, Pollack MS, Zamir R, Roitman A,
Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B: Late
onset 21‑hydroxylase deficiency and HLA in the Ashkenazi population: A
new allele at the 21‑hydroxylase locus. Human Immunol 1:55‑66, 1980.
136. Pollack MS, Levine LS, Zachmann M, Prader
A, New MI, Oberfield SE, Dupont B: Possible genetic linkage disequilibrium
between HLA and the 21‑hydroxylase deficiency gene (congenital adrenal
hyperplasia). Trans Proc XI:1315‑1316,
1979.
137. Levine LS, New MI, Pollack MS, Dupont B:
Prenatal diagnosis of congenital adrenal hyperplasia (Letter to the
Editor). Lancet 2:637, 1979.
138. New MI, Oberfield SE, Levine LS, Dupont B,
Pollack MS, Gill Jr JR, Bartter FC: Autosomal dominant transmission and absence
of HLA linkage in dexamethasone‑suppressible hyperaldosteronism (Letter
to the Editor). Lancet 1:550‑551,
1980.
139. Levine LS, Pang S, Dupont S, Pollack MS,
Lorenzen L, New MI: Detection of heterozygote of 21‑hydroxylase
deficiency (Letter to the Editor), Lancet 1:603‑604, 1980.
140. Sonino N, Levine LS, Vecsei P, New MI:
Parallelism of 11ß‑ and 18‑hydroxylation demonstrated by urinary
free hormones in man. J Clin
Endocrinol Metab 51:557‑560, 1980.
141. Sonino N, Chow D, Levine LS, New MI:
Clinical response to metyrapone as indicated by measurement of
mineralocorticoids and glucocorticoids in normal children. Clin Endocrinol (Oxf) 14:31‑39,
1981.
142. New MI, Levine LS: Low‑renin
hypertension with hyperaldosteronism in childhood, Prog Biochem Pharmacol 17:54‑57, 1980.
143. New MI, Dupont B, Levine LS: HLA and
adrenal disease. In: NR Farid (ed), HLA
in Endocrine and Metabolic Disorders, Academic Press,
144. Saenger P, Levine LS, New MI: Male
pseudohermaphroditism due to abnormal testosterone biosynthesis and metabolism,
In: SJ Kogan and ESE Hafez (eds), Clinics in Andrology, Vol 7. In: Pediatric Andrology, Martinus
Nijhoff Publishers,
145. New MI, Levine LS: Inborn errors of steroid
biosynthesis. In: HLJ Makin (ed), Biochemistry
of Steroid Hormones, Second Edition, Blackwell Scientific Publishers,
Oxford, 1984, pp 595‑632.
146. New MI,
Levine LS: Congenital adrenal hyperplasia. In:
AJ Moss (ed), Pediatrics Update: Reviews for Physicians, 1981 Edition,
Elsevier North Holland, New York, 1981, pp 223‑235.
147. New MI, Levine LS: Adrenal hyperplasia in
intersex states. In: N Josso (ed), Intersex Child, In: Z Laron (ed), Pediatric and Adolescent
Endocrinology, S Karger,
148. New MI, Levine LS: Female
pseudohermaphroditism. In: JJ Sciarra, L
Speroff, and JL Simpson (eds), Gynecology and Obstetrics, vol 5, Harper
and Row, Hagerstown, 1981, pp 1‑7.
149. Sonino N, Levine LS, New MI:
Mineralocorticoid and metabolic response to metyrapone in normotensive children
and children with dexamethasone‑suppressible and primary
hyperaldosteronism. Acta Endocrinol 98:87‑94, 1981.
150. New MI, Levine LS: Hypertension of
childhood with suppressed renin, Endocrine Reviews 1:421‑430,
1980.
151. New MI, Levine LS (guest editors):
Endocrine disorders in children. Pediatr
Ann 9:131‑173, 1980.
152. New MI, Levine LS (guest editors): Hormonal
conditions. Pediatr Ann 9:359‑405,
1980.
153. Oberfield SE, Levine LS, Rauh W, Pang S,
Gottesdiener K, New MI: Androgens in
childhood hypertension. In: E Cacciari
and A Prader (eds), Pathophysiology of Puberty: Proceedings of the
Serono Symposia, Vol 36, Academic Press, London, 1980, pp 157‑162.
154. Rauh W, Levine LS, New MI: The role of
dietary salt in juvenile hypertension, In: G Giovannelli, MI New and S Gorini
(eds), Hypertension in Children and Adolescents, Raven Press, New York, 1981, pp 35‑44.
155. New MI: Investigation of new forms of
hypertension in childhood. In: G
Giovannelli, MI New and S Gorini (eds), Hypertension in Children and
Adolescents, Raven Press, New York, 1981, pp 157‑160.
156. New MI, Levine LS: Hypertension in childhood
and adolescence. Cardiovas Rev Rep,
3:115‑122, 1982.
157. Levine LS, Dupont B, Lorenzen B, Pang S,
Pollack MS, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A,
Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R,
Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI: Cryptic 21‑hydroxylase
deficiency in families of patients with classical congenital adrenal
hyperplasia. J Clin Endocrinol Metab 51:1316‑1324, 1980.
158. Dupont B, Pollack MS, Levine LS, O'Neill
GJ, Hawkins BR, New MI: Congenital adrenal hyperplasia: Joint report from the
8th International Histocompatibility Workshop. In: PI Terasaki (ed), Histocompatibility Testing 1980, UCLA
Tissue Typing Laboratory,
159. Curtis JA, Monaghan HP, New MI, Bailey JD:
Selective hypoaldosteronism in infancy. Am
J Dis Child 137:633‑636, 1983.
160. Rifkind AB, Saenger P, Levine LS, Pareira
J, New MI: Effects of growth hormone on antipyrine kinetics in children. Clin Pharmacol Therap 30:l27‑l32,
1981.
161. New MI, Levine LS: The infant with
ambiguous genitalia. In: Syllabus
32nd Ann Postgraduate Assembly of the Endocrine Society, 1980, pp 470.
162. Kuhnle U, Chow D, Rapaport R, Pang S,
Levine LS, New MI: The 21‑hydroxylase activity in the glomerulosa and
fasciculata of the adrenal cortex in congenital adrenal hyperplasia. J Clin Endocrinol Metab 52:534‑544,
1981.
163. Mininberg DT, Levine LS, New MI: Current
concepts in congenital adrenal hyperplasia. In: Advances in the Study of Birth Defects, Chap 11, In: TVN
Persaud (ed), Genetic Disorders, Syndromology and Prenatal Diagnosis, Vol 5,MTP Press, Ltd,
165. Teitelman G, Joh TH, Park D, Brodsky M, New
MI, Reis DJ: Expression of the adrenergic phenotype in cultured fetal adrenal
medullary cells: role of intrinsic and extrinsic factors. Develop Biology 89:450‑459,
1982.
166. New MI, Dupont B, Pang S, Pollack MS,
Levine LS: An update of congenital adrenal hyperplasia. Rec Prog Horm Res 37:105‑181,
1981.
167. New MI, Levine LS, Pang S: Adrenal
androgens and growth. In: M Ritzen, A
Aperia, K Hall, A Larsson, A Zetterberg, and R Zetterstrom (eds), The
Biology of Normal Human Growth, Raven Press, New York, 1981, pp 285‑295.
168. Lee SM, Lightner E, Witte M, Oberfield SE,
Levine LS, New MI: Dexamethasone suppressible hyperaldosteronism in a child
with nephrosclerosis, Acta Endocrinol 99:251‑255, 1982.
170. Levine LS, Dupont B, Lorenzen F, Pang S,
Pollack MS, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A,
Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R,
Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI: Genetic and
hormonal characterization of cryptic 21‑hydroxylase deficiency. J Clin Endocrinol Metab 53:1193‑1198,
1981.
171. New MI, Lorenzen F, Lerner AJ, Kohn B,
Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS:
Genotyping steroid 21‑hydroxylase deficiency: hormonal reference
data. J Clin Endocrinol Metab 57:320‑326, 1983.
172. New MI, Grumbach K, Levine LS: Congenital
adrenal hyperplasia, In: AEH Emery and DL Rimoin (eds), Principles and
Practice of Medical Genetics, Churchill Livingstone, Inc,
173. Lan NC, Matulich DT, Stockigt JR, Biglieri
EG, New MI, Baxter JD: Role of steroids in various states of mineralocorticoid‑excess
hypertension: Analysis by mineralocorticoid receptor assay. In: G Giovannelli, MI New, and S Gorini
(eds), Hypertension in Children and Adolescents, Raven Press, New York,
1981, pp 165‑175.
174. Pollack MS, Levine LS, O'Neill GJ, Pang S,
Lorenzen F, Kohn B, Rondanini GF, Chiumello G, New MI, Dupont B: HLA linkage
and B14,DR1,BfS haplotype association with the genes for late onset and cryptic
21‑hydroxylase deficiency. Am J
Hum Genet 33:540‑550, 1981.
175. Rapaport R, Levine LS, Petrovic M, Wilson
T, Draznin M, Bejar RL, Johanson A, New MI: The renin‑aldosterone system
in cystic fibrosis, J Pediatrics 98:768‑771, 1981.
176. New MI, Dupont B, Pollack MS, Levine LS:
The biochemical basis for genotyping 21‑hydroxylase deficiency. Human Genetics 58:123‑127, 1981.
177. Pollack MS, New MI, O'Neill GJ, Levine LS,
Callaway C, Pang S, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G,
Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C,
Pintor C, Tato L, Barboni E, Dupont B: HLA genotypes and HLA‑linked
genetic markers in Italian patients with classical 21‑hydroxylase
deficiency. Human Genetics 58:331‑337,
1981.
178. New MI: The role of steroid hormones in the
development of low‑renin hypertension of childhood. In: JMH Loggie, MJ
Horan, AB Gruskin, AR Hohn, JB Dunbar and RJ Havlik (eds), NHLBI Workshop on
Juvenile Hypertension: Proceedings from a Symposium, Bethesda, Maryland,
May 26 ‑ 27, 1983, Biomedical Information Corp, New York, 1984, pp 283‑304.
179. Oberfield SE, Levine LS, Stoner E, Chow D,
Rauh W, Greig F, Lee SM, Lightner E, Witte M, New MI: Adrenal glomerulosa
function in patients with dexamethasone‑suppressible
hyperaldosteronism. J Clin Endocrinol
Metab 53:158‑164, 1981.
180. Kuhnle U, Rosler A, Pareira JA, Gunczler P,
Levine LS, New MI: The effects of long‑term normalization of sodium
balance on linear growth in disorders with aldosterone deficiency. Acta Endocrinol 102:577‑582,
1983.
181. New MI: Precocious puberty, In: DT Krieger
and CW Bardin (eds), Current Therapy in Endocrinology 1983‑1984, BC Decker,
182. Wachtel SS, New MI: Studies on H‑Y antigen:
The genetic basis of abnormal gonadal differentiation. In: Clinics in Andrology, Vol 7. In: SJ Kogan and ESE Hafez (eds), Pediatric
Andrology, Martinus Nijhoff Publishers,
183. Pang S, Murphey M, Levine LS, Spence DA, Leon
A, LaFranchi S,