Detalhe da pesquisa
1.
Growth hormone resistance induced by amino acid deprivation in fao cells is independent of FGF21.
Biochem Biophys Res Commun
; 709: 149811, 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38569244
2.
Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient.
Doc Ophthalmol
; 141(1): 77-88, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31997113
3.
A case of neuronal ceroid lipofuscinosis type 8 associated with central precocious puberty.
Pediatr Int
; 63(3): 338-339, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33694307
4.
Atypical clinical features of children with central nervous system tumor: Delayed diagnosis and switch in handedness.
Pediatr Int
; 58(9): 923-6, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27440052
5.
Essential Amino Acid Intake Is Required for Sustaining Serum Insulin-like Growth Factor-I Levels but Is Not Necessarily Needed for Body Growth.
Cells
; 11(9)2022 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35563827
6.
Discovery of GnIH and Its Role in Hypothyroidism-Induced Delayed Puberty.
Endocrinology
; 159(1): 62-68, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28938445
7.
Fetal Goitrous Hypothyroidism and Polyhydramnios in a Patient with Compound Heterozygous DUOXA2 Mutations.
Horm Res Paediatr
; 90(2): 132-137, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30110704
8.
Successful intrauterine therapy for fetal goitrous hypothyroidism during late gestation.
Endocr J
; 54(5): 813-7, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17917306
9.
Right testicular necrosis and left vanishing testis in a neonate.
J Pediatr Endocrinol Metab
; 20(3): 449-54, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17451086
10.
Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance.
Diabetes
; 66(10): 2713-2723, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28765322
11.
Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.
J Clin Endocrinol Metab
; 91(12): 4981-7, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16968807
12.
Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features.
Clin Pediatr Endocrinol
; 25(2): 23-35, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27212794
13.
Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.
Clin Pediatr Endocrinol
; 24(2): 37-49, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26019400
14.
Diagnostic usefulness of 3 tesla MRI of the brain for cushing disease in a child.
Clin Pediatr Endocrinol
; 20(4): 89-93, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23926401
15.
A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1.
Clin Pediatr Endocrinol
; 25(3): 111-4, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27507913
16.
A Neonatal Case of Autosomal Dominant Hypoparathyroidism without Mutation of the CASR Gene.
Clin Pediatr Endocrinol
; 17(1): 17-22, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-24790357
17.
A Case of Allgrove Syndrome with a Novel IVS7 +1 G>A Mutation of The AAAS Gene.
Clin Pediatr Endocrinol
; 21(1): 11-3, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23926405
18.
Serum glucagon-like peptide-2 levels in neonates: comparison between extremely low-birthweight infants and normal-term infants.
Pediatr Int
; 48(5): 464-9, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16970784
19.
Lymphocytic hypophysitis with central diabetes insipidus and subsequent hypopituitarism masking a suprasellar germinoma in a 13-year-old girl.
Childs Nerv Syst
; 22(10): 1338-43, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16565852
20.
A novel mutation of the arginine vasopressin receptor 2 gene in a patient with congenital nephrogenic diabetes insipidus.
Clin Pediatr Endocrinol
; 14(1): 27-33, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-24790307