Detalhe da pesquisa
1.
[S3 guidelines on diagnostics and treatment of cervical cancer: Demands on pathology]. / S3-Leitlinie Diagnostik und Therapie des Zervixkarzinoms.
Pathologe
; 36(6): 585-93, 2015 Nov.
Artigo
em Alemão
| MEDLINE | ID: mdl-26483249
2.
Virus discovery in dogs with non-suppurative encephalitis reveals a high incidence of tick-borne encephalitis virus infections in Switzerland.
Schweiz Arch Tierheilkd
; 165(10): 656-666, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37822248
3.
Genome Sequences of Rare Human Enterovirus Genotypes Recovered from Clinical Respiratory Samples in Bern, Switzerland.
Microbiol Resour Announc
; 11(9): e0027622, 2022 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35993703
4.
The skeletal muscle chloride channel in dominant and recessive human myotonia.
Science
; 257(5071): 797-800, 1992 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-1379744
5.
Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel.
Neuron
; 15(6): 1455-63, 1995 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-8845168
6.
Diagnosis, Therapy and Follow-up Care of Vulvar Cancer and its Precursors. Guideline of the DGGG and DKG (S2k-Level, AWMF Registry Number 015/059, November 2015.
Geburtshilfe Frauenheilkd
; 76(10): 1035-1049, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27765958
7.
The molecular genetic approach to "Bartter's syndrome".
J Mol Med (Berl)
; 76(5): 317-25, 1998 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-9587066
8.
A simple method for characterising syndactyly in clinical practice.
Genet Couns
; 16(3): 229-38, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16261692
9.
Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy.
Arch Neurol
; 52(1): 25-31, 1995 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-7826272
10.
Proximal myotonic myopathy with MRI white matter abnormalities of the brain.
Neurology
; 48(1): 33-7, 1997 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-9008490
11.
Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts.
Neurology
; 44(8): 1448-52, 1994 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-8058147
12.
Linkage of proximal myotonic myopathy to chromosome 3q.
Neurology
; 52(1): 170-1, 1999 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-9921867
13.
An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD).
Neuromuscul Disord
; 10(3): 178-81, 2000 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-10734264
14.
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).
Neuromuscul Disord
; 10(7): 478-80, 2000 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-10996776
15.
Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD).
Am J Med Genet
; 87(1): 23-9, 1999 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-10528242
16.
Paramyotonia congenita without paralysis on exposure to cold: a novel mutation in the SCN4A gene (Val1293Ile).
Neuroreport
; 6(15): 2001-4, 1995 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-8580427
17.
Brain disease and molecular analysis in myotonic dystrophy.
Neuroreport
; 5(18): 2549-52, 1994 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-7696601
18.
Cardiac involvement in facio-scapulo-humeral muscular dystrophy: a family study using Thallium-201 single-photon-emission-computed tomography.
J Neurol Sci
; 144(1-2): 59-63, 1996 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-8994104
19.
Human transcription factor SLUG: mutation analysis in patients with neural tube defects and identification of a missense mutation (D119E) in the Slug subfamily-defining region.
Mutat Res
; 406(2-4): 63-9, 1999 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10479723
20.
The arthritis of hemochromatosis. A review of 25 cases with special reference to chondrocalcinosis, and a comparison with patients with primary hyperparathyroidism and controls.
Clin Rheumatol
; 5(3): 317-24, 1986 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-3490947