Suchergebnisse - "Jeha, George S"

PubPharm (27)

1

Crinecerfont, a CRF1 Receptor Antagonist, Lowers Adrenal Androgens in Adolescents With Congenital Adrenal Hyperplasia

enthalten in: The Journal of clinical endocrinology and metabolism | 2023

von Newfield, R. | Sarafoglou, K. | Fechner, P. | +9

CommentIn: J Clin Endocrinol Metab. 2023 Aug 31;:. - PMID 37650613

2

Evidence of feedback regulation of C-type natriuretic peptide during Vosoritide therapy in Achondroplasia

enthalten in: Scientific reports | 2021

von Prickett, T. | Espiner, E. | Irving, M. | +8

3

Vosoritide treatment accelerates bone growth in children with achondroplasia

enthalten in: Future Rare Diseases | 2021

von Savarirayan, R. | Irving, M. | Hoover-Fong, J. | +14

4

C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia

enthalten in: The New England journal of medicine | 2019

von Savarirayan, R. | Irving, M. | Bacino, C. | +16

CommentIn: N Engl J Med. 2019 Sep 26;381(13):1291. - PMID 31553847

5

Congenital hyperinsulinism as the presenting feature of Kabuki syndrome : clinical and molecular characterization of 9 affected individuals

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2019

von Yap, K. | Johnson, A. | Fischer, D. | +22

ErratumIn: Genet Med. 2018 Aug 11;:. - PMID 30097611

6

Correction : "Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals"

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2019

von Yap, K. | Johnson, A. | Fischer, D. | +22

ErratumFor: Genet Med. 2019 Jan;21(1):233-242. - PMID 29907798

7

A Novel Intragenic SLC16A1 Mutation Associated With Congenital Hyperinsulinism

enthalten in: Global pediatric health | 2017

von Tosur, M. | Jeha, G.

8

Persistent Diabetes Mellitus Postadrenalectomy in Neonatal McCune-Albright Syndrome

enthalten in: Global pediatric health | 2017

von Tosur, M. | Collins, M. | Ponder, S. | +3

9

Infantile Growth Hormone Deficiency and X- Linked Adrenal Hypoplasia Congenita

enthalten in: Jacobs journal of pediatrics | 2015

von Chung, S. | Chi, C. | Haymond, M. | +1

10

Activation of cyclic AMP signaling leads to different pathway alterations in lesions of the adrenal cortex caused by germline PRKAR1A defects versus those due to somatic GNAS mutations

enthalten in: The Journal of clinical endocrinology and metabolism | 2012

von Almeida, M. | Azevedo, M. | Xekouki, P. | +11