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...

Recommendations for the management of galactosaemia

Archives of disease in childhood, 1999-01, Vol.80 (1), p.93-96

1999

Volltextzugriff (PDF)

Clinical approach to treatable inborn metabolic diseases: An introduction

Journal of inherited metabolic disease, 2006-04, Vol.29 (2-3), p.261-274

2006

Volltextzugriff (PDF)

How practical are recommendations for dietary control in phenylketonuria?

The Lancet (British edition), 2002-07, Vol.360 (9326), p.55-57

2002

Volltextzugriff (PDF)

Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study

Arteriosclerosis, thrombosis, and vascular biology, 2001-12, Vol.21 (12), p.2080-2085

2001

Volltextzugriff (PDF)

Maternal phenylketonuria: report from the United Kingdom Registry 1978–97

Archives of disease in childhood, 2005-02, Vol.90 (2), p.143-146

2005

Volltextzugriff (PDF)

L‐Carnitine in inborn errors of metabolism: What is the evidence?

Journal of inherited metabolic disease, 2003-01, Vol.26 (2-3), p.181-188

Walter, J. H.

2003

Volltextzugriff (PDF)

The management of organic acidaemias: The role of transplantation

Journal of inherited metabolic disease, 2001-04, Vol.24 (2), p.309-311

2001

Volltextzugriff (PDF)

Pyruvate dehydrogenase E3 binding protein (protein X) deficiency

Developmental medicine and child neurology, 2006-09, Vol.48 (9), p.756-760

2006

Volltextzugriff (PDF)

Arguments for early screening: a clinician's perspective

European journal of pediatrics, 2003-12, Vol.162 Suppl 1, p.S2-S4

Walter, John H

2003

Volltextzugriff (PDF)

The use of amino acid supplements in inherited metabolic disease

Journal of inherited metabolic disease, 2006-04, Vol.29 (2-3), p.279-280

2006

Volltextzugriff (PDF)

Pyruvate dehydrogenase deficiency presenting as dystonia in childhood

Developmental medicine and child neurology, 2004-10, Vol.46 (10), p.710-712

2004

Volltextzugriff (PDF)

Inborn errors of metabolism and pregnancy

Journal of inherited metabolic disease, 2000-05, Vol.23 (3), p.229-236

Walter, J. H.

2000

Volltextzugriff (PDF)

The impact of screening for propionic and methylmalonic acidaemia

European journal of pediatrics, 2003-12, Vol.162 Suppl 1, p.S21-S24

2003

Volltextzugriff (PDF)

L-Carnitine

Archives of Disease in Childhood, 1996-06, Vol.74 (6), p.475-478

Walter, J H

1996

Volltextzugriff (PDF)

Increased risk of vitamin B12 deficiency in patients with phenylketonuria on an unrestricted or relaxed diet

The Journal of pediatrics, 2000-04, Vol.136 (4), p.545-547

2000

Volltextzugriff (PDF)

The benefits of liver transplantation in glycogenosis type Ib

Journal of inherited metabolic disease, 2004-07, Vol.27 (4), p.539-540

2004

Volltextzugriff (PDF)

Feeding infants with undiluted goat's milk can mimic tyrosinaemia type 1

Acta Paediatrica, 2004-04, Vol.93 (4), p.552-553

2004

Volltextzugriff (PDF)

Generalised uridine diphosphate galactose-4-epimerase deficiency

Archives of disease in childhood, 1999-04, Vol.80 (4), p.374-376

1999

Volltextzugriff (PDF)

Cytokeratins in the canine epidermis

Veterinary dermatology, 2001-04, Vol.12 (2), p.81-87

Walter, J.H

2001

Volltextzugriff (PDF)

Dietary compliance in ornithine aminotransferase deficiency

Journal of inherited metabolic disease, 2006-02, Vol.29 (1), p.240-240

2006

Volltextzugriff (PDF)

Magnetic resonance imaging of the brain in phenylketonuria

The Lancet (British edition), 1994-07, Vol.344 (8915), p.87-90

1994

Volltextzugriff (PDF)

Strategies for the treatment of cystathionine beta-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years

European journal of pediatrics, 1998-04, Vol.157 Suppl 2 (S2), p.S71-S76

1998

Volltextzugriff (PDF)

A patient satisfaction survey on prescription custom-molded foot orthoses

Journal of the American Podiatric Medical Association, 2004-07, Vol.94 (4), p.363-367

2004

Volltextzugriff (PDF)

Magnetic resonance imaging in phenylketonuria: Reversal of cerebral white matter change

The Journal of pediatrics, 1995-08, Vol.127 (2), p.251-255

1995

Volltextzugriff (PDF)

Prolidase deficiency and systemic lupus erythematosus

Archives of disease in childhood, 1997-05, Vol.76 (5), p.441-444

1997

Volltextzugriff (PDF)

1 – 25 von 882

Menü

Weitere Dienste

Einstellungen

Recommendations for the management of galactosaemia

Clinical approach to treatable inborn metabolic diseases: An introduction

How practical are recommendations for dietary control in phenylketonuria?

Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study

Maternal phenylketonuria: report from the United Kingdom Registry 1978–97

L‐Carnitine in inborn errors of metabolism: What is the evidence?

The management of organic acidaemias: The role of transplantation

Pyruvate dehydrogenase E3 binding protein (protein X) deficiency

Arguments for early screening: a clinician's perspective

The use of amino acid supplements in inherited metabolic disease

Pyruvate dehydrogenase deficiency presenting as dystonia in childhood

Inborn errors of metabolism and pregnancy

The impact of screening for propionic and methylmalonic acidaemia

L-Carnitine

Increased risk of vitamin B12 deficiency in patients with phenylketonuria on an unrestricted or relaxed diet

The benefits of liver transplantation in glycogenosis type Ib

Feeding infants with undiluted goat's milk can mimic tyrosinaemia type 1

Generalised uridine diphosphate galactose-4-epimerase deficiency

Cytokeratins in the canine epidermis

Dietary compliance in ornithine aminotransferase deficiency

Magnetic resonance imaging of the brain in phenylketonuria

Strategies for the treatment of cystathionine beta-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years

A patient satisfaction survey on prescription custom-molded foot orthoses

Magnetic resonance imaging in phenylketonuria: Reversal of cerebral white matter change

Prolidase deficiency and systemic lupus erythematosus

Suchergebnisse filtern