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1.
Serum NT-proCNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia.
Clin Endocrinol (Oxf)
; 84(6): 845-50, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-26814021
2.
Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects.
J Clin Endocrinol Metab
; 2024 Feb 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-38373250
3.
Pathogenic variants of the GNAS gene introduce an abnormal amino acid sequence in the ß6 strand/α5 helix of Gsα, causing pseudohypoparathyroidism type 1A and pseudopseudohypoparathyroidism in two unrelated Japanese families.
Bone Rep
; 17: 101637, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36407415
4.
Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report.
Clin Pediatr Endocrinol
; 28(1): 1-7, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30745727
5.
A novel heterozygous T51I mutation of growth hormone receptor is not associated with short stature.
Growth Horm IGF Res
; 12(6): 411-7, 2002 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-12423626
6.
Clinical Trial of Four Weeks of Combination Therapy with Low-dose Methimazole and a Cholesterol Absorption Inhibitor as the Initial Treatment for Childhood-onset Graves' Disease.
Clin Pediatr Endocrinol
; 23(1): 17-25, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24532957
7.
Premature thelarche in later childhood demonstrates a pubertal response to GnRH stimulation test at one year after breast development.
Clin Pediatr Endocrinol
; 20(4): 81-7, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23926400
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