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...

Skeletal muscle sonography: a correlative study of echogenicity and morphology

Journal of ultrasound in medicine, 1993-02, Vol.12 (2), p.73-77

1993

Volltextzugriff (PDF)

Glycogenosis type V (McArdle's disease) mimicking atypical myositis

Clinical rheumatology, 2001, Vol.20 (1), p.57-60

2001

Volltextzugriff (PDF)

Therapy of complex I deficiency : peripheral neuropathy during dichloroacetate therapy

European journal of pediatrics, 1995-11, Vol.154 (11), p.928-932

1995

Volltextzugriff (PDF)

Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency

Archives of pathology & laboratory medicine (1976), 1993-02, Vol.117 (2), p.202

1993

Volltextzugriff (PDF)

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria

European journal of pediatrics, 1993-08, Vol.152 (8), p.665-670

1993

Volltextzugriff (PDF)

Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency

Journal of neurology, 1991-02, Vol.238 (1), p.31-33

1991

Volltextzugriff (PDF)

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies

Virchows Archiv A Pathological Anatomy and Histopathology, 1991-01, Vol.419 (4), p.355-362

1991

Volltextzugriff (PDF)

Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose

Klinische Wochenschrift, 1986-12, Vol.64 (24), p.1281-1290

1986

Volltextzugriff (PDF)

Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR)]

FEBS letters, 1991-07, Vol.286 (1-2), p.67-70

1991

Volltextzugriff (PDF)

Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome

Brain & development (Tokyo. 1979), 1995-03, Vol.17 (2), p.117-121

1995

Volltextzugriff (PDF)

Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency

Virchows Archiv. Abteilung B. Zellpathologie, 1985, Vol.48 (2), p.185-196

1985

Volltextzugriff (PDF)

Activation of the pyruvate dehydrogenase complex in isolated fat cell mitochondria by hydrogen peroxide and t-butyl hydroperoxide

FEBS letters, 1980-12, Vol.122 (1), p.29-32

1980

Volltextzugriff (PDF)

Studies on the interference by haemoglobin in the determination of bilirubin

Journal of clinical chemistry and clinical biochemistry, 1983-07, Vol.21 (7), p.437

1983

Volltextzugriff (PDF)

Myoglobinuria and carnitine palmitoyltransferase deficiency. Diagnostic procedure and differential diagnosis

Wiener Klinische Wochenschrift, 1994, Vol.106 (6), p.174-177

1994

Volltextzugriff (PDF)

Serum Carnitine During Valproic Acid Therapy

Epilepsia (Copenhagen), 1986-10, Vol.27 (5), p.559-562

1986

Volltextzugriff (PDF)

Activation of pyruvate dehydrogenase by insulin in isolated brown fat cells

Hormone and metabolic research, 1979-04, Vol.11 (4), p.285

1979

Volltextzugriff (PDF)

Reference ranges for carnitine in muscle, serum, and urine of newborn infants and children

Fresenius' Zeitschrift für analytische Chemie, 1986-01, Vol.324 (3-4), p.291-292

1986

Volltextzugriff (PDF)

Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry

Klinische Wochenschrift, 1984-07, Vol.62 (14), p.651-658

1984

Volltextzugriff (PDF)

Diagnostic significance of muscle biopsies in metabolic myopathies. I. Myopathology

Klinische Wochenschrift, 1984-07, Vol.62 (13), p.603-612

1984

Volltextzugriff (PDF)

Insulin activates pyruvate dehydrogenase by lowering the mitochondrial acetyl-CoA/CoA ratio as evidenced by digitonin fraction of isolated fat cells

FEBS letters, 1978-09, Vol.93 (2), p.307-311

1978

Volltextzugriff (PDF)

Insulin activates pyruvate dehydrogenase by lowering the mitochondrial acetyl-CoA/CoA ratio as evidenced by digitonin fractionation of isolated fat cells

FEBS letters, 1978-09, Vol.93 (2), p.307-311

1978

Volltextzugriff (PDF)

Diagnostische Bedeutung von Muskelbiopsien bei metabolischen Myopathien: II. Klinische biochemie

Klinische Wochenschrift, 1984-07, Vol.62 (14), p.651-658

1984

Volltextzugriff (PDF)

Diagnostische Bedeutung von Muskelbiopsien bei metabolischen Myopathien: I. Myopathologie

Klinische Wochenschrift, 1984-07, Vol.62 (13), p.603-612

1984

Volltextzugriff (PDF)

Influence of individual factors on fundamental diagrams of pedestrians

Physica A, 2022-06, Vol.595, p.127077, Article 127077

2022

Volltextzugriff (PDF)

Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies

Journal of clinical chemistry and clinical biochemistry, 1990-04, Vol.28 (4), p.241

1990

Volltextzugriff (PDF)

1 – 25 von 46

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(36)
Mit Volltextzugriff
(33)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Skeletal muscle sonography: a correlative study of echogenicity and morphology

Glycogenosis type V (McArdle's disease) mimicking atypical myositis

Therapy of complex I deficiency : peripheral neuropathy during dichloroacetate therapy

Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria

Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies

Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose

Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR)]

Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome

Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency

Activation of the pyruvate dehydrogenase complex in isolated fat cell mitochondria by hydrogen peroxide and t-butyl hydroperoxide

Studies on the interference by haemoglobin in the determination of bilirubin

Myoglobinuria and carnitine palmitoyltransferase deficiency. Diagnostic procedure and differential diagnosis

Serum Carnitine During Valproic Acid Therapy

Activation of pyruvate dehydrogenase by insulin in isolated brown fat cells

Reference ranges for carnitine in muscle, serum, and urine of newborn infants and children

Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry

Diagnostic significance of muscle biopsies in metabolic myopathies. I. Myopathology

Insulin activates pyruvate dehydrogenase by lowering the mitochondrial acetyl-CoA/CoA ratio as evidenced by digitonin fraction of isolated fat cells

Insulin activates pyruvate dehydrogenase by lowering the mitochondrial acetyl-CoA/CoA ratio as evidenced by digitonin fractionation of isolated fat cells

Diagnostische Bedeutung von Muskelbiopsien bei metabolischen Myopathien: II. Klinische biochemie

Diagnostische Bedeutung von Muskelbiopsien bei metabolischen Myopathien: I. Myopathologie

Influence of individual factors on fundamental diagrams of pedestrians

Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies

Suchergebnisse filtern