UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 511

Sortiert nach

The assay of phenylacetic acid and 4-phenylbutyric acid in physiological fluids

Clinica chimica acta, 1999-06, Vol.284 (1), p.109-111

Hommes, Frits A

1999

Link zum Volltext

Verfügbarkeit prüfen

Loss of neurotransmitter receptors by hyperphenylalaninemia in the HPH-5 mouse brain

Acta Paediatrica, 1994-12, Vol.83 (s407), p.120-121

Hommes, FA

1994

Link zum Volltext

Verfügbarkeit prüfen

Abnormal oligosaccharide pattern in glycogen storage disease type III

Journal of inherited metabolic disease, 1996-01, Vol.19 (3), p.383-384

1996

Link zum Volltext

Verfügbarkeit prüfen

Quality control for selective screening of inborn errors of metabolism

European journal of pediatrics, 1994, Vol.153 (7 Suppl 1), p.S17-S22

Hommes, F A

1994

Link zum Volltext

Verfügbarkeit prüfen

The role of the blood‐brain barrier in the aetiology of permanent brain dysfunction in hyperphenylalaninaemia

Journal of inherited metabolic disease, 1989-03, Vol.12 (1), p.41-46

Hommes, F. A.

1989

Link zum Volltext

Verfügbarkeit prüfen

High-performance liquid chromatography of urinary oligosaccharides in the diagnosis of glycoprotein degradation disorders

Clinica chimica acta, 1991-12, Vol.203 (2), p.211-224

1991

Link zum Volltext

Verfügbarkeit prüfen

N‐acetylglutamate synthetase deficiency: Clinical and laboratory observations

Journal of inherited metabolic disease, 1991-09, Vol.14 (5), p.685-690

1991

Link zum Volltext

Verfügbarkeit prüfen

Purification and some properties of liver adenylylsulfate kinase

Biochimica et biophysica acta, 1987-05, Vol.924 (2), p.270-275

1987

Link zum Volltext

Verfügbarkeit prüfen

The control of 5‐hydroxytryptamine and dopamine synthesis in the brain: A theoretical approach

Journal of inherited metabolic disease, 1990-01, Vol.13 (1), p.37-57

1990

Link zum Volltext

Verfügbarkeit prüfen

Adult-onset chorea and dementia with propionic acidemia

Neurology, 1989-10, Vol.39 (10), p.1343

1989

Link zum Volltext

Verfügbarkeit prüfen

Amino acidaemias and brain maturation: Interference with sulphate activation and myelin metabolism

Journal of inherited metabolic disease, 1985-06, Vol.8 (S2), p.121-122

Hommes, F. A.

1985

Link zum Volltext

Verfügbarkeit prüfen

On a possible mechanism of abnormal brain development in experimental hyperphenylalaninemia

Neurochemistry international, 1987, Vol.11 (1), p.1-10

1987

Link zum Volltext

Verfügbarkeit prüfen

The effect of hyperphenylalaninaemia on the muscarinic acetylcholine receptor in the HPH‐5 mouse brain

Journal of inherited metabolic disease, 1993-11, Vol.16 (6), p.962-974

Hommes, F. A.

1993

Link zum Volltext

Verfügbarkeit prüfen

An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosis

Journal of medical genetics, 1992-06, Vol.29 (6), p.423-424

1992

Link zum Volltext

Verfügbarkeit prüfen

Biotin

World review of nutrition and dietetics, 1986, Vol.48, p.34

Hommes, F A

1986

Link zum Volltext

Verfügbarkeit prüfen

Biochemical observations on a case of hepatic fructose‐1,6‐diphosphatase deficiency

Journal of inherited metabolic disease, 1985-12, Vol.8 (4), p.169-173

1985

Link zum Volltext

Verfügbarkeit prüfen

Myelin turnover in hyperphenylalaninaemia. A re‐evaluation with the HPH‐5 mouse

Journal of inherited metabolic disease, 1992-03, Vol.15 (2), p.243-251

1992

Link zum Volltext

Verfügbarkeit prüfen

Properties of the 3'-phosphoadenosine-5'-phosphosulfate (PAPS) synthesizing systems of brain and liver

Neurochemical research, 1987-04, Vol.12 (4), p.345-349

1987

Link zum Volltext

Verfügbarkeit prüfen

Inborn errors of fructose metabolism

The American journal of clinical nutrition, 1993-11, Vol.58 (5), p.788S-795S

Hommes, FA

1993

Link zum Volltext

Verfügbarkeit prüfen

The assay of ATP-sulfurylase

Analytical biochemistry, 1986-04, Vol.154 (1), p.100-103

1986

Link zum Volltext

Verfügbarkeit prüfen

Reconstitution of ornithine transport in liposomes with Lubrol extracts of mitochondria

FEBS letters, 1984-05, Vol.170 (1), p.131-134

1984

Link zum Volltext

Verfügbarkeit prüfen

Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)

Neuropediatrics, 1986-02, Vol.17 (1), p.48

1986

Link zum Volltext

Verfügbarkeit prüfen

Ultrastructural changes in fibroblast mitochondria of a patient with HHH‐syndrome

Journal of inherited metabolic disease, 1984-12, Vol.7 (4), p.147-150

1984

Link zum Volltext

Verfügbarkeit prüfen

Anticonvulsive drugs and blood levels of lactate, pyruvate, and glucose in children with seizures

Neurology, 1986-09, Vol.36 (9), p.1267

1986

Link zum Volltext

Verfügbarkeit prüfen

HPLC assay of phenylalanine and tyrosine in blood spots on filter paper

Clinica chimica acta, 1986-04, Vol.156 (1), p.91-96

1986

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 511

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(445)
Mit Volltextzugriff
(401)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(314)
Life Sciences & Biomedicine
(280)
Humans
(220)
Female
(139)
Male
(134)
Biological And Medical Sciences
(130)
Medical Sciences
(113)
Animals
(97)
Adult
(94)
Middle Aged
(70)
Rats
(54)
Biochemistry & Molecular Biology
(49)
Gastroenterology & Hepatology
(49)
Neurosciences & Neurology
(49)
Clinical Neurology
(39)
Aged
(35)
Pediatrics
(35)
Neurology
(31)
Pharmacology. Drug Treatments
(30)
Gastroenterology. Liver. Pancreas. Abdomen
(29)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The assay of phenylacetic acid and 4-phenylbutyric acid in physiological fluids

Loss of neurotransmitter receptors by hyperphenylalaninemia in the HPH-5 mouse brain

Abnormal oligosaccharide pattern in glycogen storage disease type III

Quality control for selective screening of inborn errors of metabolism

The role of the blood‐brain barrier in the aetiology of permanent brain dysfunction in hyperphenylalaninaemia

High-performance liquid chromatography of urinary oligosaccharides in the diagnosis of glycoprotein degradation disorders

N‐acetylglutamate synthetase deficiency: Clinical and laboratory observations

Purification and some properties of liver adenylylsulfate kinase

The control of 5‐hydroxytryptamine and dopamine synthesis in the brain: A theoretical approach

Adult-onset chorea and dementia with propionic acidemia

Amino acidaemias and brain maturation: Interference with sulphate activation and myelin metabolism

On a possible mechanism of abnormal brain development in experimental hyperphenylalaninemia

The effect of hyperphenylalaninaemia on the muscarinic acetylcholine receptor in the HPH‐5 mouse brain

An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosis

Biotin

Biochemical observations on a case of hepatic fructose‐1,6‐diphosphatase deficiency

Myelin turnover in hyperphenylalaninaemia. A re‐evaluation with the HPH‐5 mouse

Properties of the 3'-phosphoadenosine-5'-phosphosulfate (PAPS) synthesizing systems of brain and liver

Inborn errors of fructose metabolism

The assay of ATP-sulfurylase

Reconstitution of ornithine transport in liposomes with Lubrol extracts of mitochondria

Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)

Ultrastructural changes in fibroblast mitochondria of a patient with HHH‐syndrome

Anticonvulsive drugs and blood levels of lactate, pyruvate, and glucose in children with seizures

HPLC assay of phenylalanine and tyrosine in blood spots on filter paper

Suchergebnisse filtern