Detalhe da pesquisa
1.
Stage III Chorioamnionitis is Associated with Reduced Risk of Severe Retinopathy of Prematurity.
J Pediatr
; 272: 114085, 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38703992
2.
Radiological characteristics of skeletal growth in neonates and infants with achondroplasia.
Am J Med Genet A
; 194(5): e63525, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38158382
3.
A novel pathogenic variant p.Asp797Val in IFIH1 in a Japanese boy with overlapping Singleton-Merten syndrome and Aicardi-Goutières syndrome.
Am J Med Genet A
; 188(1): 249-252, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34453469
4.
Urinary Protein-to-creatinine Ratios Predict Recurrence in Pediatric and Young Adult Cases of Minimal Change Nephrotic Syndrome.
Acta Med Okayama
; 76(1): 41-49, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35236997
5.
Chemoradiotherapy for Unresectable INI1-negative Chordoma in a Child.
J Pediatr Hematol Oncol
; 42(1): 65-68, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30281526
6.
Laboratory changes during adrenocorticotropic hormone therapy associated with renal calcified lesions.
Pediatr Int
; 62(5): 587-592, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31957090
7.
Recurrent Meningitis in an 11-year-old Girl with a Petrous Apex Cystic Lesion.
Acta Med Okayama
; 72(5): 519-523, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30369610
8.
Changes in the features of invasive pneumococcal disease after introduction of the seven-valent pneumococcal conjugate vaccine in a regional core hospital of Kochi, Japan.
Acta Med Okayama
; 69(4): 255-60, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26289917
9.
Novel and recurrent COMP gene variants in five Japanese patients with pseudoachondroplasia: skeletal changes from the neonatal to infantile periods.
Clin Pediatr Endocrinol
; 32(4): 221-227, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37842142
10.
Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders.
J Bone Miner Res
; 38(5): 692-706, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36896612
11.
Rapid Progression of Heterotopic Ossification in Severe Variant of Fibrodysplasia Ossificans Progressiva with p.Arg258Gly in ACVR1: A Case Report and Review of Clinical Phenotypes.
Case Rep Genet
; 2022: 5021758, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36060212
12.
Thioredoxin interacting protein protects mice from fasting induced liver steatosis by activating ER stress and its downstream signaling pathways.
Sci Rep
; 12(1): 4819, 2022 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35314758
13.
Vitamin B6 in acute encephalopathy with biphasic seizures and late reduced diffusion.
Brain Dev
; 42(5): 402-407, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32107100
14.
Differential diagnosis of nonepileptic twilight state with convulsive manifestations after febrile seizures.
Brain Dev
; 40(9): 781-785, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29866486
15.
Efficient conversion of mannitol derived from brown seaweed to fructose for fermentation with a thraustochytrid.
J Biosci Bioeng
; 125(2): 180-184, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28970111
16.
Author Correction: Thioredoxin interacting protein protects mice from fasting induced liver steatosis by activating ER stress and its downstream signaling pathways.
Sci Rep
; 12(1): 8026, 2022 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35577819
17.
Emphysematous cholecystitis with massive gas in the abdominal cavity.
World J Gastroenterol
; 19(4): 604-6, 2013 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382645
18.
A Japanese case of hereditary chin trembling responsive to arotinolol.
Parkinsonism Relat Disord
; 29: 133-4, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27117562