Detalhe da pesquisa
1.
Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data.
Am J Med Genet A
; : e63612, 2024 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38554024
2.
Clinical characteristics of and growth hormone treatment effects on short stature with type 1 insulin-like growth factor receptor (IGF1R) gene alteration.
Endocr J
; 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710621
3.
Thyroid hormone may predict treatment failure in Kawasaki disease.
Pediatr Int
; 66(1): e15723, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38326932
4.
Step-by-step protocol for alternative injury models in newt cardiac regeneration.
Dev Growth Differ
; 65(5): 266-271, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37155321
5.
Cryo-injury procedure-induced cardiac regeneration shows unique gene expression profiles in the newt Pleurodeles waltl.
Dev Dyn
; 251(5): 864-876, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34964213
6.
Photoperiod-independent testicular development in the model newt Pleurodeles waltl.
Dev Growth Differ
; 63(6): 277-284, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34133763
7.
Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia.
Calcif Tissue Int
; 108(5): 622-633, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33484279
8.
Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial.
Lancet
; 393(10189): 2416-2427, 2019 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31104833
9.
DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations.
Cytogenet Genome Res
; 158(2): 56-62, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31158835
10.
Functional analysis of monocarboxylate transporter 8 mutations in Japanese Allan-Herndon-Dudley syndrome patients.
Endocr J
; 66(1): 19-29, 2019 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30369548
11.
Pyridoxal 5'-phosphate and related metabolites in hypophosphatasia: Effects of enzyme replacement therapy.
Mol Genet Metab
; 125(1-2): 174-180, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30049651
12.
Final adult height in long-term growth hormone-treated achondroplasia patients.
Eur J Pediatr
; 176(7): 873-879, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28501952
13.
A high-risk alveolar rhabdomyosarcoma case with Duchenne muscular dystrophy.
Pediatr Int
; 64(1): e14754, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34757683
14.
Serum NT-proCNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia.
Clin Endocrinol (Oxf)
; 84(6): 845-50, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26814021
15.
Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reports.
Am J Med Genet A
; 170A(2): 426-434, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26567084
16.
[FGF23 related hypophosphatemic rickets:current therapy and unresolved issues].
Clin Calcium
; 26(2): 269-76, 2016 Feb.
Artigo
em Japonês
| MEDLINE | ID: mdl-26813507
17.
Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatment.
Endocr J
; 62(9): 811-6, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26135520
18.
Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.
Am J Med Genet A
; 164A(1): 156-63, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24259409
19.
Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature.
Eur J Pediatr
; 173(6): 799-804, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24390061
20.
Changes in University Hospital Physicians' Work and Family Lives Following Outsourcing of Housework Cleaning Tasks.
Yonago Acta Med
; 67(1): 75-79, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38371279