UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Vibrational behavior investigation approach and Influence of contact coefficient on stator natural frequencies

2017 18th International Symposium on Electromagnetic Fields in Mechatronics, Electrical and Electronic Engineering (ISEF) Book of Abstracts, 2017, p.1-2

2017

Volltextzugriff (PDF)

Ataxia with vitamin E deficiency : refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families

American journal of human genetics, 1995-05, Vol.56 (5), p.1116-1124

1995

Volltextzugriff (PDF)

Limb-girdle muscular dystrophy 2C: Clinical aspects

Neuromuscular disorders : NMD, 1996-12, Vol.6 (6), p.493-494

1996

Volltextzugriff (PDF)

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)

American journal of human genetics, 1995-09, Vol.57 (3), p.732-734

1995

Volltextzugriff (PDF)

Prevalence of Epilepsy in Kelibia, Tunisia

Epilepsia (Copenhagen), 1993-11, Vol.34 (6), p.1028-1032

1993

Volltextzugriff (PDF)

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

Human molecular genetics, 1994, Vol.3 (10), p.1867-1871

1994

Volltextzugriff (PDF)

Recessive Schwartz-Jampel syndrome (SJS) : confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval

Human genetics, 1996-09, Vol.98 (3), p.380-385

1996

Volltextzugriff (PDF)

Giant Axonal Neuropathy Locus Refinement To A < 590 KB Critical Interval

Journal of the peripheral nervous system, 2001-03, Vol.6 (1), p.60-60

2001

Volltextzugriff (PDF)

Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval

American journal of human genetics, 1994-06, Vol.54 (6), p.1050-1059

1994

Volltextzugriff (PDF)

Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred

Neurology, 1990-02, Vol.40 (2), p.245-245

1990

Volltextzugriff (PDF)

Prevalence study of neurologic disorders in Kelibia (Tunisia)

Neuroepidemiology, 1993, Vol.12 (5), p.285-299

1993

Volltextzugriff (PDF)

Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A

Genomics (San Diego, Calif.), 1995-07, Vol.28 (2), p.286-290

1995

Volltextzugriff (PDF)

Calculation of the optical and electronic properties of TiNx thin films on domain IR–VIS–UV

Journal of molecular structure. Theochem, 2006-11, Vol.777 (1-3), p.41-44

2006

Volltextzugriff (PDF)

Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy

Neurology, 1990-12, Vol.40 (12), p.1903-1903

1990

Volltextzugriff (PDF)

Infantile dermatomyositis. Study of 8 personal cases

Annales de pediatrie, 1967-08, Vol.14 (8), p.554

1967

Volltextzugriff (PDF)

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus

American journal of human genetics, 1992-12, Vol.51 (6), p.1372-1376

1992

Volltextzugriff (PDF)

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy

Muscle & nerve, 1994-04, Vol.17 (4), p.400-410

1994

Volltextzugriff (PDF)

Calculation of the optical and electronic properties of TiN x thin films on domain IR–VIS–UV

Journal of molecular structure. Theochem, 2006, Vol.777 (1), p.41-44

2006

Volltextzugriff (PDF)

Fungal Mycotic aneurysms and visceral infection due to Scedosporium apiospermum in a kidney transplant patient

Transplantation proceedings, 1993-06, Vol.25 (3), p.2290-2291

1993

Volltextzugriff (PDF)

Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus

Clinical neuroscience (New York, N.Y.), 1995, Vol.3 (1), p.39

1995

Volltextzugriff (PDF)

Public health issues and clinical and neurological characteristics of the new variant of Creutzfeldt-Jakob disease and other human and animal transmissible spongiform encephalopathies: memorandum from two WHO meetings

Bulletin of the World Health Organization, 1996-09, Vol.74 (5), p.453-463

1996

Volltextzugriff (PDF)

Schwartz-Jampel syndrome. Clinical and histopathological study of 4 cases

Revue neurologique, 1991, Vol.147 (4), p.279-284

1991

Volltextzugriff (PDF)

Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein Po

Annals of neurology, 1992-11, Vol.32 (5), p.700-702

1992

Volltextzugriff (PDF)

Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome

Journal of the neurological sciences, 1991-07, Vol.104 (1), p.64-73

1991

Volltextzugriff (PDF)

Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum

Neuromuscular disorders : NMD, 1992, Vol.2 (5), p.361-369

1992

Volltextzugriff (PDF)

26 – 50 von 185

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(147)
Mit Volltextzugriff
(130)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Vibrational behavior investigation approach and Influence of contact coefficient on stator natural frequencies

Ataxia with vitamin E deficiency : refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families

Limb-girdle muscular dystrophy 2C: Clinical aspects

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)

Prevalence of Epilepsy in Kelibia, Tunisia

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

Recessive Schwartz-Jampel syndrome (SJS) : confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval

Giant Axonal Neuropathy Locus Refinement To A < 590 KB Critical Interval

Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval

Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred

Prevalence study of neurologic disorders in Kelibia (Tunisia)

Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A

Calculation of the optical and electronic properties of TiNx thin films on domain IR–VIS–UV

Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy

Infantile dermatomyositis. Study of 8 personal cases

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy

Calculation of the optical and electronic properties of TiN x thin films on domain IR–VIS–UV

Fungal Mycotic aneurysms and visceral infection due to Scedosporium apiospermum in a kidney transplant patient

Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus

Public health issues and clinical and neurological characteristics of the new variant of Creutzfeldt-Jakob disease and other human and animal transmissible spongiform encephalopathies: memorandum from two WHO meetings

Schwartz-Jampel syndrome. Clinical and histopathological study of 4 cases

Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein Po

Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome

Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum

Suchergebnisse filtern