UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 296

Sortiert nach

Clinical presentations of mitochondrial cardiomyopathies

Pediatric cardiology, 2004-09, Vol.25 (5), p.443-450

2004

Volltextzugriff (PDF)

Critical phenomena in complex contagions

Social networks, 2012-10, Vol.34 (4), p.451-461

2012

Volltextzugriff (PDF)

Reduced body fat and increased hepatic lipid synthesis in mice bearing interleukin-6-secreting tumor

American journal of physiology: endocrinology and metabolism, 2001-11, Vol.281 (5), p.E957-E965

2001

Volltextzugriff (PDF)

A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion

European journal of paediatric neurology, 2008-07, Vol.12 (4), p.309-313

2008

Volltextzugriff (PDF)

Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency

Molecular genetics and metabolism, 2003-08, Vol.79 (4), p.288-293

2003

Volltextzugriff (PDF)

Multiple presentation of mitochondrial disorders

Archives of disease in childhood, 1999-09, Vol.81 (3), p.209-215

1999

Volltextzugriff (PDF)

Magneto-optical current sensor by domain wall motion in orthoferrites

IEEE transactions on instrumentation and measurement, 2000-02, Vol.49 (1), p.14-18

2000

Volltextzugriff (PDF)

Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: Possible beneficial effect of vitamin therapy

Journal of inherited metabolic disease, 2003-01, Vol.26 (8), p.816-818

2003

Volltextzugriff (PDF)

Insulin resistance in the NIDDM model Psammomys obesus in the normoglycaemic, normoinsulinaemic state

Diabetologia, 1996-11, Vol.39 (11), p.1269-1275

1996

Volltextzugriff (PDF)

Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levels

American journal of physiology: endocrinology and metabolism, 1997-08, Vol.273 (2), p.E262-E267

1997

Volltextzugriff (PDF)

Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/intron 5 junction point mutation: a unique disorder or the natural course of this glycolytic disorder?

Neurology, 1994-06, Vol.44 (6), p.1097

1994

Volltextzugriff (PDF)

Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients

Annals of neurology, 1991-11, Vol.30 (5), p.655-662

1991

Volltextzugriff (PDF)

Complex I deficiency with diabetes, Fanconi syndrome and mtDNA deletion

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.298-300

1994

Volltextzugriff (PDF)

The frequency of the C854 mutation in the aspartoacylase gene in Ashkenazi Jews in Israel

American journal of human genetics, 1994-08, Vol.55 (2), p.287-288

1994

Volltextzugriff (PDF)

Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome

The Journal of pediatrics, 1995, Vol.126 (1), p.72-74

1995

Volltextzugriff (PDF)

Faraday effect in yttrium orthoferrite in the range 1280–1600 nm

Journal of magnetism and magnetic materials, 1995-11, Vol.151 (1), p.207-210

1995

Volltextzugriff (PDF)

Magnetic field sensor by orthoferrites

Sensors and actuators. A. Physical., 1997-04, Vol.59 (1-3), p.56-60

1997

Volltextzugriff (PDF)

Subsonic domain wall dynamics in yttrium orthoferrite

Journal of magnetism and magnetic materials, 1998, Vol.177, p.203-204

1998

Volltextzugriff (PDF)

Physical exercise enhances hepatic insulin signaling and inhibits phosphoenolpyruvate carboxykinase activity in diabetes-prone Psammomys obesus

Metabolism, clinical and experimental, 2004-07, Vol.53 (7), p.836-841

2004

Volltextzugriff (PDF)

Metabolic effects of nicotine on human adipose tissue in organ culture

Journal of molecular medicine (Berlin, Germany), 1994, Vol.72 (2), p.94-99

1994

Volltextzugriff (PDF)

Neurologic Presentations of Mitochondrial Disorders

Journal of child neurology, 2000-01, Vol.15 (1), p.44-48

2000

Volltextzugriff (PDF)

Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency

Journal of inherited metabolic disease, 1991-11, Vol.14 (6), p.902-907

1991

Volltextzugriff (PDF)

Fetal diabetes in rats and its effect on placental glycogen

Diabetologia, 1985-04, Vol.28 (4), p.244-249

1985

Volltextzugriff (PDF)

3‐Hydroxy‐3‐methylglutaryl‐coenzyme A lyase deficiency: Biochemical studies and family investigation of four generations

Journal of inherited metabolic disease, 1990-03, Vol.13 (2), p.156-164

1990

Volltextzugriff (PDF)

Mechanism of placental glycogen deposition in diabetes in the rat

Diabetologia, 1983-01, Vol.24 (1), p.63-68

1983

Volltextzugriff (PDF)

1 – 25 von 296

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(260)
Mit Volltextzugriff
(234)

Publikationsform

Sprache

Englisch
(254)
Russisch
(44)
Japanisch
(18)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Clinical presentations of mitochondrial cardiomyopathies

Critical phenomena in complex contagions

Reduced body fat and increased hepatic lipid synthesis in mice bearing interleukin-6-secreting tumor

A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion

Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency

Multiple presentation of mitochondrial disorders

Magneto-optical current sensor by domain wall motion in orthoferrites

Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: Possible beneficial effect of vitamin therapy

Insulin resistance in the NIDDM model Psammomys obesus in the normoglycaemic, normoinsulinaemic state

Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levels

Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/intron 5 junction point mutation: a unique disorder or the natural course of this glycolytic disorder?

Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients

Complex I deficiency with diabetes, Fanconi syndrome and mtDNA deletion

The frequency of the C854 mutation in the aspartoacylase gene in Ashkenazi Jews in Israel

Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome

Faraday effect in yttrium orthoferrite in the range 1280–1600 nm

Magnetic field sensor by orthoferrites

Subsonic domain wall dynamics in yttrium orthoferrite

Physical exercise enhances hepatic insulin signaling and inhibits phosphoenolpyruvate carboxykinase activity in diabetes-prone Psammomys obesus

Metabolic effects of nicotine on human adipose tissue in organ culture

Neurologic Presentations of Mitochondrial Disorders

Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency

Fetal diabetes in rats and its effect on placental glycogen

3‐Hydroxy‐3‐methylglutaryl‐coenzyme A lyase deficiency: Biochemical studies and family investigation of four generations

Mechanism of placental glycogen deposition in diabetes in the rat

Suchergebnisse filtern