H. Globerman

发表

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.

P. White, M. New, K. Parker, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Nonsense mutation causing steroid 21-hydroxylase deficiency.

P. White, M. New, K. Parker, 1988, The Journal of clinical investigation.

Analysis of the peroxisome proliferator activated receptor gamma (PPARgamma) gene in HAIRAN syndrome with obesity.

C. Yen, A. Shuldiner, C. Harel, 2000, Clinical endocrinology.

An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylase.

P. White, M. New, A. Rösler, 1988, The New England journal of medicine.

Expression and purification of functional human 17 alpha-hydroxylase/17,20-lyase (P450c17) in Escherichia coli. Use of this system for study of a novel form of combined 17 alpha-hydroxylase/17,20-lyase deficiency.

M. Waterman, N. Kagawa, H. Globerman, 1993, The Journal of biological chemistry.

Inhibin B in Men with Severe Obesity and After Weight Reduction Following Gastroplasty

E. Karnieli, Z. Shen-Orr, I. Charuzi, 2005, Endocrine research.

A xanthogranulomatous histiocytosis in a child presenting with short stature.

P. Winchester, H. Globerman, S. Frankel, 1991, The American journal of pediatric hematology/oncology.

Analysis of the insulin receptor gene tyrosine kinase domain in obese patients with hyperandrogenism, insulin resistance and acanthosis nigricans (type C insulin resistance)

E. Karnieli, H. Globerman, 1998, International Journal of Obesity.

Analysis of the peroxisome proliferator activated receptor γ (PPARγ) gene in HAIRAN syndrome with obesity

A. Shuldiner, A. Shuldiner, C. Harel, 2000 .

Eosinophilic Granuloma Presenting as Hypothyroidism and Goiter

E. Grabowski, M. New, J. Felix, 1989 .

Haemolysis in a G6PD-deficient child induced by eating unripe peaches.

M. Chevion, H. Globerman, T. Navok, 2009, Scandinavian journal of haematology.