Detalhe da pesquisa
1.
The use of ultrasound in central vascular ligation during laparoscopic right-sided colon cancer surgery: technical notes.
Tech Coloproctol
; 25(10): 1155-1161, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34095976
2.
Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetes.
Diabet Med
; 37(12): 2131-2135, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31872455
3.
Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool.
Hum Reprod
; 34(9): 1762-1769, 2019 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31398259
4.
NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy.
Clin Genet
; 93(5): 1103-1106, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29344937
5.
Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes.
Diabet Med
; 35(3): 376-380, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29247561
6.
Catastrophic cellular events leading to complex chromosomal rearrangements in the germline.
Clin Genet
; 91(5): 653-660, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27888607
7.
Incidence and prevalence of childhood-onset Type 1 diabetes in Japan: the T1D study.
Diabet Med
; 34(7): 909-915, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27925270
8.
FUT2 non-secretor status is associated with Type 1 diabetes susceptibility in Japanese children.
Diabet Med
; 34(4): 586-589, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27859559
9.
Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader-Willi syndrome due to UPD(15)mat.
Clin Genet
; 89(5): 614-9, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26526156
10.
Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21.
Diabet Med
; 33(12): 1717-1722, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27352912
11.
Locomotive Syndrome: Operational Definition Based on a Questionnaire, and Exercise Interventions on Mobility Dysfunction in Elderly People.
Clin Rev Bone Miner Metab
; 14: 119-130, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27375372
12.
A New Statistical Model Identified Two-thirds of Clinical T1 Gastric Cancers as Possible Candidates for Endoscopic Treatment.
Ann Surg Oncol
; 22(7): 2317-22, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25752893
13.
Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients.
Hum Reprod
; 30(3): 499-506, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25605705
14.
Mechanical and neural changes in plantar-flexor muscles after spinal cord injury in humans.
Spinal Cord
; 53(7): 526-33, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25665544
15.
Diagnostic value of computed tomography for staging of clinical T1 gastric cancer.
Ann Surg Oncol
; 21(9): 3002-7, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24687153
16.
A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
Clin Genet
; 86(6): 539-44, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24299031
17.
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.
Nat Genet
; 16(1): 54-63, 1997 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-9140395
18.
Construction of self-cloning bottom-fermenting yeast with low vicinal diketone production by the homo-integration of ILV5.
Yeast
; 29(10): 435-42, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23038161
19.
46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism.
Clin Genet
; 82(6): 505-13, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22288726
20.
Case of anti-glomerular basement membrane antibody-induced glomerulonephritis with cytomegalovirus-induced thrombotic microangiopathy.
Intern Med J
; 42(3): e7-e11, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22432999