Detalhe da pesquisa
1.
Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.
Eur J Neurol
; 24(2): 427-e6, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28102045
2.
Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.
Clin Genet
; 74(2): 116-26, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18477000
3.
Novel features in a patient homozygous for the L347P mutation in the PINK1 gene.
Parkinsonism Relat Disord
; 13(6): 359-61, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17055324
4.
Elevated α-synuclein caused by SNCA gene triplication impairs neuronal differentiation and maturation in Parkinson's patient-derived induced pluripotent stem cells.
Cell Death Dis
; 6: e1994, 2015 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26610207
5.
Phase-I trial of intravenous continuous infusion of tumor necrosis factor in advanced metastatic carcinomas.
J Cancer Res Clin Oncol
; 115(2): 189-92, 1989.
Artigo
em Inglês
| MEDLINE | ID: mdl-2654135
6.
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers.
Neurology
; 77(4): 325-33, 2011 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21753163
7.
[Pediatric intensive care in Ulm]. / Kinderintensivpflege in Ulm.
Kinderkrankenschwester
; 18(8): 337, 1999 Aug.
Artigo
em Alemão
| MEDLINE | ID: mdl-10531949
8.
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.
Neurology
; 68(12): 916-22, 2007 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-17251522
9.
[Review of the results of the ARO multicenter study]. / Uberblick und Ergebnisse der ARO-Multicenterstudie.
Orthopade
; 27(6): 324-32, 1998 Jun.
Artigo
em Alemão
| MEDLINE | ID: mdl-9697139
10.
[Radiologic results of the ARO multicenter study]. / Die Radiologischen Ergebnisse der ARO-Multicenterstudie.
Orthopade
; 27(6): 333-40, 1998 Jun.
Artigo
em Alemão
| MEDLINE | ID: mdl-9697140
11.
[Implant failure after total hip replacement. Comparison of patients with primary coxarthrosis, rheumatoid arthritis and dysplastic coxarthrosis]. / Implantatversager nach Hüft-TEP-Implantation. Vergleich bei Patienten mit primärer Koxarthrose, rheumatischer Arthritis und Dysplasiekoxarthrose.
Orthopade
; 27(6): 341-8, 1998 Jun.
Artigo
em Alemão
| MEDLINE | ID: mdl-9697141
12.
[Follow-up control of ultrasonographic neonatal screening of the hip]. / Verlaufskontrollen von Hüftbefunden im sonographischen Neugeborenenscreening.
Ultraschall Med
; 20(4): 161-4, 1999 Aug.
Artigo
em Alemão
| MEDLINE | ID: mdl-10522359
13.
[Pyogenic spondylitis in the interarticular portion of the vertebral arch. Case report on primary dorsal spondylitis]. / Die pyogene Spondylitis in der Interartikularportion des Wirbelbogens. Kasuistischer Beitrag zu den primär dorsalen S pondylitiden.
Z Orthop Ihre Grenzgeb
; 134(2): 185-8, 1996.
Artigo
em Alemão
| MEDLINE | ID: mdl-8779265
14.
Conspicuous enterocytic binding pattern for peanut lectin and malignant histiocytosis of the intestine.
Virchows Arch A Pathol Anat Histopathol
; 399(2): 245-53, 1983.
Artigo
em Inglês
| MEDLINE | ID: mdl-6404054
15.
The distribution of fibronectin in lymph nodes infiltrated by Hodgkin's disease. An immunoperoxidase study on paraffin sections.
Virchows Arch A Pathol Anat Histopathol
; 400(3): 319-29, 1983.
Artigo
em Inglês
| MEDLINE | ID: mdl-6412441
16.
J-chain-producing immunoblastic lymphoma in a case of Richter's syndrome. Immunohistochemical evidence for a gradual malignant transformation of a single B-cell clone and flow cytophotometric data.
Virchows Arch A Pathol Anat Histol
; 396(2): 213-24, 1982.
Artigo
em Inglês
| MEDLINE | ID: mdl-6812283
17.
[Heparin-induced thrombocytopenia after elective hip joint replacement with postoperative prevention of thromboembolism with low-molecular-weight heparin]. / Heparin-induzierte Thrombozytopenie nach elektivem Hüftgelenksersatz unter einer postoperativen Thromboembolieprophylaxe mit niedermolekularem Heparin.
Z Orthop Ihre Grenzgeb
; 137(6): 536-9, 1999.
Artigo
em Alemão
| MEDLINE | ID: mdl-10666863
18.
Genetic heterogeneity in ten families with myoclonus-dystonia.
J Neurol Neurosurg Psychiatry
; 75(8): 1181-5, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15258227
19.
[A 54-year-old patient with muscle weakness, hypokalemia and arterial hypertension]. / 54jährige Patientin mit Muskelschwäche, Hypokaliämie und arterieller Hypertonie.
Internist (Berl)
; 29(10): 697-9, 1988 Oct.
Artigo
em Alemão
| MEDLINE | ID: mdl-3069781
20.
Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutations.
Neurology
; 62(7): 1229-31, 2004 Apr 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-15079037