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...

Mastitis control in bred dairy heifers using dry cow therapy and teat sealant to prevent new infections and to cure existing ones

Applied Animal Science, 2020-02, Vol.36 (1), p.91-99

2020

Volltextzugriff (PDF)

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms

Nucleic acids research, 1989-06, Vol.17 (12), p.4465-4469

1989

Volltextzugriff (PDF)

Spinocerebellar degeneration associated with a selective defect of vitamin E absorption

The New England journal of medicine, 1985-07, Vol.313 (1), p.32-35

1985

Volltextzugriff (PDF)

The mitochondrial genome--breaking the magic circle

The New England journal of medicine, 1989-05, Vol.320 (20), p.1341-1343

Harding, A E

1989

Volltextzugriff (PDF)

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

The Lancet (British edition), 1992-12, Vol.340 (8832), p.1376-1379

1992

Volltextzugriff (PDF)

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

The Lancet (British edition), 1992-06, Vol.339 (8806), p.1375-1377

1992

Volltextzugriff (PDF)

CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS

The Lancet (British edition), 1983-05, Vol.321 (8334), p.1151-1155

Harding, A.E.

1983

Volltextzugriff (PDF)

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I

American journal of human genetics, 1994-06, Vol.54 (6), p.959-965

1994

Volltextzugriff (PDF)

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

The Lancet (British edition), 1991-06, Vol.337 (8753), p.1311-1313

1991

Volltextzugriff (PDF)

Neurological disease and mitochondrial genes

Trends in neurosciences (Regular ed.), 1991-04, Vol.14 (4), p.132-138

Harding, A.E.

1991

Volltextzugriff (PDF)

Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene

QJM : An International Journal of Medicine, 1993-11

1993

Volltextzugriff (PDF)

Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features

Journal of the neurological sciences, 1996-11, Vol.143 (1), p.41-45

1996

Volltextzugriff (PDF)

DIAGNOSIS OF GERSTMANN-STRÄUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS

The Lancet (British edition), 1989-07, Vol.334 (8653), p.15-17

1989

Volltextzugriff (PDF)

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy

American journal of human genetics, 1992-10, Vol.51 (4), p.741-748

1992

Volltextzugriff (PDF)

Platelet mitochondrial function in Leber's hereditary optic neuropathy

Journal of the neurological sciences, 1994-03, Vol.122 (1), p.80-83

1994

Volltextzugriff (PDF)

Demyelination following diphtheria toxin in the presence of axonal atrophy

Journal of the neurological sciences, 1984-05, Vol.64 (2), p.199-211

1984

Volltextzugriff (PDF)

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

The Lancet (British edition), 1994-09, Vol.344 (8924), p.714-717

1994

Volltextzugriff (PDF)

Smoking and mitochondrial function : a model for environmental toxins

QJM : An International Journal of Medicine, 1993-10, Vol.86 (10), p.657-660

1993

Volltextzugriff (PDF)

Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study

Journal of the neurological sciences, 1995-07, Vol.131 (1), p.78-87

1995

Volltextzugriff (PDF)

NOTICES OF RECENT PUBLICATIONS

Brain (London, England : 1878), 1984, Vol.107 (2), p.657-658

HARDING, A.E.

1984

Volltextzugriff (PDF)

Evidence for Locus Heterogeneity in Autosomal Dominant Torsion Dystonia

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.9-12

1993

Volltextzugriff (PDF)

Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA

Journal of the neurological sciences, 1995-06, Vol.130 (2), p.154-160

1995

Volltextzugriff (PDF)

Neurogenetics update

Journal of the neurological sciences, 1994-10, Vol.126 (1), p.90-93

Harding, A.E.

1994

Volltextzugriff (PDF)

‘Idiopathic’ late onset cerebellar ataxia

Journal of the neurological sciences, 1981-08, Vol.51 (2), p.259-271

Harding, A.E.

1981

Volltextzugriff (PDF)

Antibodies to human optic nerve in Leber's hereditary optic neuropathy

Journal of the neurological sciences, 1995-06, Vol.130 (2), p.134-138

1995

Volltextzugriff (PDF)

1 – 25 von 83

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(73)
Mit Volltextzugriff
(67)

Publikationsform

Sprache

Englisch
(83)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mastitis control in bred dairy heifers using dry cow therapy and teat sealant to prevent new infections and to cure existing ones

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms

Spinocerebellar degeneration associated with a selective defect of vitamin E absorption

The mitochondrial genome--breaking the magic circle

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

Neurological disease and mitochondrial genes

Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene

Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features

DIAGNOSIS OF GERSTMANN-STRÄUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy

Platelet mitochondrial function in Leber's hereditary optic neuropathy

Demyelination following diphtheria toxin in the presence of axonal atrophy

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

Smoking and mitochondrial function : a model for environmental toxins

Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study

NOTICES OF RECENT PUBLICATIONS

Evidence for Locus Heterogeneity in Autosomal Dominant Torsion Dystonia

Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA

Neurogenetics update

‘Idiopathic’ late onset cerebellar ataxia

Antibodies to human optic nerve in Leber's hereditary optic neuropathy

Suchergebnisse filtern