M. I. New

发表

Methionyl human growth hormone and oxandrolone in Turner syndrome: preliminary results of a prospective randomized trial.

J. Frane, S. Chernausek, P. Saenger, 1986, The Journal of pediatrics.

Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia.

S. Pang, M. I. New, J. Hotchkiss, 1977, The Journal of clinical endocrinology and metabolism.

Growth and final height in classical and nonclassical 21-hydroxylase deficiency.

M. New, P. Speiser, P. del Balzo, 1989, Journal of endocrinological investigation.

Serum androgens in normal prepubertal and pubertal children and in children with precocious adrenarche.

M. New, L. Levine, S. Korth-Schutz, 1976, The Journal of clinical endocrinology and metabolism.

Genetic defects of steroidogenesis in premature pubarche.

M. New, J. Temeck, S. Pang, 1987, The Journal of clinical endocrinology and metabolism.

MOLECULAR BASIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 3β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY

J. Simard, M. New, É. Rhéaume, 1993, Pediatric Research.

Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women.

M. New, E. Stoner, S. Oberfield, 1985, The Journal of clinical endocrinology and metabolism.

Long term outcome in adult males with classic congenital adrenal hyperplasia.

M. Vogiatzi, M. S. Cabrera, M. I. New, 2001, The Journal of clinical endocrinology and metabolism.

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

B. Kohn, M. New, B. Dupont, 1981, American journal of human genetics.

Maternal age as a risk factor for hypospadias.

T. Hensle, M. New, G. Hyun, 2001, The Journal of urology.

Evaluation of the dexamethasone suppression test for the diagnosis of glucocorticoid-remediable aldosteronism.

R. Lifton, M. New, R. Dluhy, 1997, The Journal of clinical endocrinology and metabolism.

An abnormality in steroid reductive metabolism in a hypertensive syndrome.

M. New, L. Ramirez, S. Ulick, 1977, The Journal of clinical endocrinology and metabolism.

SERUM ANDROGEN CONCENTRATIONS IN NEONATES AND YOUNG INFANTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 21‐HYDROXYLASE DEFICIENCY *

M. New, C. Faiman, S. Pang, 1979, Clinical endocrinology.

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

B. Kohn, C. Scaroni, M. New, 1980, The Journal of clinical endocrinology and metabolism.

The interrelationship of sodium balance, plasma renin activity and ACTH in congenital adrenal hyperplasia.

M. New, A. Rösler, L. Levine, 1977, The Journal of clinical endocrinology and metabolism.

Disorders of gonadal differentiation and congenital adrenal hyperplasia.

M. New, N. Josso, M. I. New, 1988, Endocrinology and metabolism clinics of North America.