Detalhe da pesquisa
1.
Growth and Bone Mineral Density Changes in Ovariectomized Rats Treated with Estrogen Receptor Alpha or Beta Agonists.
J Korean Med Sci
; 35(45): e370, 2020 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-33230983
2.
Phenotypic and molecular spectrum of Korean patients with Lesch-Nyhan syndrome and attenuated clinical variants.
Metab Brain Dis
; 34(5): 1335-1340, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31129767
3.
DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea.
J Korean Med Sci
; 32(6): 1042-1045, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28480665
4.
Short-term efficacy of N-carbamylglutamate in a patient with N-acetylglutamate synthase deficiency.
J Hum Genet
; 60(7): 395-7, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25787344
5.
Diverse genetic aetiologies and clinical outcomes of paediatric hypoparathyroidism.
Clin Endocrinol (Oxf)
; 83(6): 790-6, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26384470
6.
Genetic polymorphism of SMAD5 is associated with Kawasaki disease.
Pediatr Cardiol
; 35(4): 601-7, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24163009
7.
The Prevalence of Abdominal Obesity and Metabolic Syndrome in Korean Children and Adolescents.
J Obes Metab Syndr
; 32(2): 103-105, 2023 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37311703
8.
Near final height in Korean children referred for evaluation of short stature: clinical utility and analytical validity of height prediction methods.
Ann Pediatr Endocrinol Metab
; 23(1): 28-32, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29609446
9.
Variable Clinical Characteristics and Molecular Spectrum of Patients with Syndromes of Reduced Sensitivity to Thyroid Hormone: Genetic Defects in the THRB and SLC16A2 Genes.
Horm Res Paediatr
; 90(5): 283-290, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30497070
10.
Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty.
Ann Pediatr Endocrinol Metab
; 21(3): 136-142, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27777905
11.
Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A.
Ann Pediatr Endocrinol Metab
; 21(3): 169-173, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27777911
12.
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.
Korean J Pediatr
; 59(1): 16-23, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26893599
13.
Endocrine dysfunctions in children with Williams-Beuren syndrome.
Ann Pediatr Endocrinol Metab
; 21(1): 15-20, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27104174
14.
Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndrome.
Ann Pediatr Endocrinol Metab
; 21(1): 26-30, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27104176
15.
Phelan-McDermid syndrome presenting with developmental delays and facial dysmorphisms.
Korean J Pediatr
; 59(Suppl 1): S25-S28, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28018439
16.
Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience.
Ann Pediatr Endocrinol Metab
; 20(1): 27-33, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25883924
17.
Turner syndrome presented with tall stature due to overdosage of the SHOX gene.
Ann Pediatr Endocrinol Metab
; 20(2): 110-3, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26191517
18.
Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency.
Ann Pediatr Endocrinol Metab
; 19(1): 32-5, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24926461
19.
Long-term follow-up on Cushing disease patient after transsphenoidal surgery.
Ann Pediatr Endocrinol Metab
; 19(3): 164-8, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25346922