Detalhe da pesquisa
1.
Longitudinal data of serum creatine kinase levels and motor, pulmonary, and cardiac functions in 337 patients with Duchenne muscular dystrophy.
Muscle Nerve
; 69(5): 604-612, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38511270
2.
Nail-patella syndrome with nephropathy in a de novo LMX1B mutation: triangular lunula of the thumb and lack of finger creases as clues.
Pediatr Nephrol
; 2024 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38478172
3.
Factors related to recurrence of proteinuria in childhood IgA nephropathy.
Pediatr Nephrol
; 39(2): 463-471, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37594578
4.
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children.
Pediatr Nephrol
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38662234
5.
Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome.
Clin Exp Nephrol
; 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658441
6.
Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial).
Clin Exp Nephrol
; 28(4): 337-348, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38010466
7.
Recurrent transient severe hypocalcaemia in two siblings with type 1 Bartter syndrome.
Nephrology (Carlton)
; 29(3): 164-167, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38062639
8.
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.
Kidney Int
; 103(5): 962-972, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36898413
9.
Clinical and laboratory characteristics of complex febrile seizures in the acute phase: a case-series study in Japan.
BMC Neurol
; 23(1): 28, 2023 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36653748
10.
Time course of serum cytokine level changes within 72 h after onset in children with acute encephalopathy and febrile seizures.
BMC Neurol
; 23(1): 7, 2023 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36609211
11.
Clinical and pathological investigation of oligomeganephronia.
Pediatr Nephrol
; 38(3): 757-762, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35861872
12.
Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective study.
Pediatr Nephrol
; 38(7): 2107-2116, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36449102
13.
Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis.
Pediatr Nephrol
; 38(12): 4023-4031, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37380934
14.
Investigation of the current situation regarding diagnosis and treatment of Alport syndrome in Asian countries: results of survey of the Asian Paediatric Nephrology association (AsPNA) tubular and inherited working group.
Clin Exp Nephrol
; 27(9): 776-780, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37289334
15.
Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene.
Clin Exp Nephrol
; 27(3): 218-226, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36371577
16.
All reported non-canonical splice site variants in GLA cause aberrant splicing.
Clin Exp Nephrol
; 27(9): 737-746, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254000
17.
Association of Familial Fanconi Syndrome with a Novel GATM Variant.
Tohoku J Exp Med
; 260(4): 337-340, 2023 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37286521
18.
X-linked Alport Syndrome with Type IV Collagen α5 Chain Staining Revealing Normal Expression in the Glomerular Basement Membrane and Negative on Bowman's Capsule and Distal Tubular Basement Membrane: A Case Report.
Tohoku J Exp Med
; 261(1): 69-73, 2023 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37495524
19.
Mycophenolate Mofetil after Rituximab for Childhood-Onset Complicated Frequently-Relapsing or Steroid-Dependent Nephrotic Syndrome.
J Am Soc Nephrol
; 33(2): 401-419, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34880074
20.
Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome.
J Obstet Gynaecol Res
; 49(6): 1624-1627, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36907825