Detalhe da pesquisa
1.
Low association between fasting and OGTT stimulated glucose levels with HbA1c in overweight children and adolescents.
Pediatr Diabetes
; 18(8): 734-741, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27873429
2.
Diabetes screening in overweight and obese children and adolescents: choosing the right test.
Eur J Pediatr
; 176(1): 89-97, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27888412
3.
Hormonal 'minipuberty' influences the somatic development of boys but not of girls up to the age of 6 years.
Clin Endocrinol (Oxf)
; 83(5): 694-701, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26031777
4.
Potential for Optimization of Growth Hormone Treatment in Children with Growth Hormone Deficiency (GHD), Small for Gestational Age (SGA), and Turner Syndrome (TS) in Germany - Data from the PATRO® Children Study.
Horm Res Paediatr
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38663373
5.
Cross-sectional analysis: clinical presentation of children with persistently low ALP levels.
J Pediatr Endocrinol Metab
; 34(12): 1559-1566, 2021 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34428361
6.
Increased Insulin Concentrations During Growth Hormone Treatment in Girls With Turner Syndrome Are Ameliorated by Hormone Replacement Therapy.
Front Endocrinol (Lausanne)
; 11: 586055, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33381083
7.
Safety and Effectiveness of Omnitrope®, a Biosimilar Recombinant Human Growth Hormone: More Than 10 Years' Experience from the PATRO Children Study.
Horm Res Paediatr
; 93(3): 154-163, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32814319
8.
Sex hormone testosterone affects language organization in the infant brain.
Neuroreport
; 19(3): 283-6, 2008 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-18303567
9.
Long-term GnRH agonist treatment for female central precocious puberty does not impair reproductive function.
Mol Cell Endocrinol
; 254-255: 217-20, 2006 Jul 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-16757104
10.
The residue E351 is essential for the activity of human 21-hydroxylase: evidence from a naturally occurring novel point mutation compared with artificial mutants generated by single amino acid substitutions.
J Mol Med (Berl)
; 83(7): 561-8, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15830218
11.
Prevalence of autoantibodies associated with thyroid and celiac disease in Ullrich-Turner syndrome in relation to adult height after growth hormone treatment.
J Pediatr Endocrinol Metab
; 19(2): 149-54, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16562588
12.
Acceptance of a reusable self-injection device for recombinant human growth hormone: final data from a questionnaire-based, cross-sectional, international, multicenter, observational study in pediatric patients.
Med Devices (Auckl)
; 9: 317-24, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27660496
13.
Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita.
Hum Mutat
; 25(5): 502-3, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15841486
14.
Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
J Clin Endocrinol Metab
; 90(1): 445-54, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15483094
15.
Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene.
J Clin Endocrinol Metab
; 90(6): 3724-30, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15755848
16.
Homozygous disruption of P450 side-chain cleavage (CYP11A1) is associated with prematurity, complete 46,XY sex reversal, and severe adrenal failure.
J Clin Endocrinol Metab
; 90(1): 538-41, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15507506
17.
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.
J Clin Endocrinol Metab
; 90(3): 1323-31, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15613420
18.
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.
Eur J Endocrinol
; 152(4): 515-9, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15817905
19.
Gonadotropin-releasing hormone analogue treatment for precocious puberty. Twenty years of experience.
Endocr Dev
; 8: 94-125, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15722620
20.
Treatment of central precocious puberty and early puberty with GnRH analog in girls with Williams-Beuren syndrome.
J Pediatr Endocrinol Metab
; 28(11-12): 1363-7, 2015 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26197460