Detalhe da pesquisa
1.
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males.
Eur J Neurol
; 21(1): 49-56, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-23724928
2.
Expression of CD64 on polymorphonuclear neutrophils in patients with familial Mediterranean fever.
Clin Exp Immunol
; 164(3): 365-72, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21438869
3.
Hypothermia in VGKC antibody-associated limbic encephalitis.
J Neurol Neurosurg Psychiatry
; 79(2): 202-4, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18202210
4.
An effective chemotherapeutic regimen for acute myeloid leukemia and myelodysplastic syndrome in children with Down's syndrome.
Leukemia
; 14(5): 786-91, 2000 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-10803507
5.
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.
J Neuropathol Exp Neurol
; 59(12): 1070-86, 2000 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11138927
6.
Complete neurological recovery of an adult patient with type II citrullinemia after living related partial liver transplantation.
Transplantation
; 62(11): 1679-84, 1996 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-8970629
7.
Detection of bcr/abl fusion transcripts by semiquantitative multiplex RT-PCR combined with a colormetric assay in Ph positive leukemia.
Cancer Lett
; 124(2): 173-80, 1998 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-9500207
8.
Successful prevention of hematological relapse for a patient with Philadelphia chromosome-positive acute lymphoblastic leukemia after allogeneic bone marrow transplantation by donor leukocyte infusion.
Bone Marrow Transplant
; 19(4): 393-4, 1997 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-9051252
9.
Generation of HLA-A2 subtype specific cytotoxic T lymphocytes from cord blood used for cord blood stem cell transplantation.
Bone Marrow Transplant
; 26(4): 451-3, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10982294
10.
Detection of donor lymphocytes in the cerebrospinal fluid of a patient with metachromatic leukodystrophy following bone marrow transplantation.
Bone Marrow Transplant
; 15(1): 137-9, 1995 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-7742747
11.
A novel minor histocompatibility antigen recognized by HLA-A31 restricted cytotoxic T lymphocytes generated from HLA-identical bone marrow donor lymphocytes.
Bone Marrow Transplant
; 24(2): 129-37, 1999 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-10455340
12.
Correlation of regional cerebral blood flow with performance on neuropsychological tests in schizophrenic patients.
Schizophr Res
; 3(4): 241-6, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2278985
13.
Nodular cutaneous amyloidosis and carpal tunnel syndrome due to the amyloidogenic transthyretin His 114 variant.
Amyloid
; 8(2): 105-10, 2001 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-11409031
14.
Biological characteristics and prognostic value of in vitro three-drug resistance to prednisolone, L-asparaginase, and vincristine in childhood acute lymphoblastic leukemia.
Int J Hematol
; 70(4): 268-77, 1999 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-10643153
15.
Distinctive multidrug sensitivity and outcome of acute erythroblastic and megakaryoblastic leukemia in children with Down syndrome.
Int J Hematol
; 74(4): 428-36, 2001 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11794699
16.
Mutation of potential N-linked glycosylation sites in the Alzheimer's disease amyloid precursor protein (APP).
Neurosci Lett
; 221(1): 57-60, 1996 Dec 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-9014180
17.
A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis.
J Neurol Sci
; 156(1): 30-4, 1998.
Artigo
em Inglês
| MEDLINE | ID: mdl-9559983
18.
Familial frontotemporal dementia with a P301L tau mutation in Japan.
J Neurol Sci
; 176(1): 57-64, 2000 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-10865093
19.
Life-threatening orthostatic hypotension in a case with bulbo-myelo-radiculo-neuropathy.
Auton Neurosci
; 94(1-2): 125-31, 2001 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-11775701
20.
An 80-year-old mitochondrial disease patient with A3243G tRNA(Leu(UUR)) gene presenting cardiac dysfunction as the main symptom.
Intern Med
; 40(5): 405-8, 2001 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-11393411