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...

Erythropoiesis and iron metabolism in dominant erythropoietic protoporphyria

Blood, 2007-12, Vol.110 (12), p.4108-4110

2007

Volltextzugriff (PDF)

The origin and spread of the HFE-C282Y haemochromatosis mutation

Human genetics, 2004-09, Vol.115 (4), p.269-279

2004

Volltextzugriff (PDF)

Haptoglobin: a review of the major allele frequencies worldwide and their association with diseases

International journal of laboratory hematology, 2007-04, Vol.29 (2), p.92-110

2007

Volltextzugriff (PDF)

Co-Inheritance of Mutations in the Uroporphyrinogen Decarboxylase and Hemochromatosis Genes Accelerates the Onset of Porphyria Cutanea Tarda

Journal of investigative dermatology, 2000-11, Vol.115 (5), p.868-874

2000

Volltextzugriff (PDF)

Serum transferrin receptor assays and their application

Annals of clinical biochemistry, 2002-05, Vol.39 (Pt 3), p.221-230

Worwood, Mark

2002

Volltextzugriff (PDF)

Inherited iron loading: genetic testing in diagnosis and management

Blood reviews, 2005-03, Vol.19 (2), p.69-88

Worwood, Mark

2005

Volltextzugriff (PDF)

Iron regulatory protein 1 and 2 in human monocytes, macrophages and duodenum: expression and regulation in hereditary hemochromatosis and iron deficiency

Haematologica (Roma), 2006-03, Vol.91 (3), p.289B-289B

Worwood, Mark

2006

Volltextzugriff (PDF)

A WHO Reference Reagent for the Serum Transferrin Receptor (sTfR): international collaborative study to evaluate a recombinant soluble transferrin receptor preparation

Clinical chemistry and laboratory medicine, 2010-06, Vol.48 (6), p.815-820

2010

Volltextzugriff (PDF)

Soluble transferrin receptor and iron homeostasis

Haematologica (Roma), 2005-01, Vol.90 (1), p.2-2

Worwood, Mark

2005

Volltextzugriff (PDF)

The laboratory assessment of iron status — an update

Clinica Chimica Acta, 1997-03, Vol.259 (1), p.3-23

Worwood, Mark

1997

Volltextzugriff (PDF)

Diet and genetic factors associated with iron status in middle-aged women

The American journal of clinical nutrition, 2005-10, Vol.82 (4), p.813-820

2005

Volltextzugriff (PDF)

Autosomal dominant reticuloendothelial iron overload associated with a 3–base pair deletion in the ferroportin 1 gene(SLC11A3)

Blood, 2002-07, Vol.100 (2), p.695-697

2002

Volltextzugriff (PDF)

HFE Mutations as risk factors in disease

Best practice & research. Clinical haematology, 2002-06, Vol.15 (2), p.295-314

Worwood, Mark

2002

Volltextzugriff (PDF)

Automated immunoassay methods for ferritin: recovery studies to assess traceability to an international standard

Clinical chemistry and laboratory medicine, 2008-10, Vol.46 (10), p.1450-1457

2008

Volltextzugriff (PDF)

Hereditary hemochromatosis gene (HFE) variants are associated with birth weight and childhood leukemia risk

Pediatric blood & cancer, 2009-12, Vol.53 (7), p.1242-1248

2009

Volltextzugriff (PDF)

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

The Lancet (British edition), 1997-02, Vol.349 (9048), p.321-323

1997

Volltextzugriff (PDF)

Headache as a presenting symptom in hereditary hemachromatosis [corrected]

Annals of neurology, 2003-01, Vol.53 (1), p.145; author reply 145-145; author reply 146

2003

Volltextzugriff (PDF)

The limited value of methylmalonic acid, homocysteine and holotranscobalamin in the diagnosis of early B12 deficiency

Haematologica (Roma), 2006-02, Vol.91 (2), p.231-234

2006

Volltextzugriff (PDF)

HFE mutations as risk factors in disease: Iron metabolism

Best practice & research. Clinical haematology, 2002, Vol.15 (2), p.295-314

WORWOOD, Mark

2002

Volltextzugriff (PDF)

HFE gene mutations in susceptibility to childhood leukemia: HuGE review

Genetics in medicine, 2005-03, Vol.7 (3), p.159-168

2005

Volltextzugriff (PDF)

Hereditary haemochromatosis: only 1% of adult HFE C282Y homozygotes in South Wales have a clinical diagnosis of iron overload

Human genetics, 2002-12, Vol.111 (6), p.538-543

2002

Volltextzugriff (PDF)

Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis

British journal of haematology, 2003-07, Vol.122 (2), p.326-332

2003

Volltextzugriff (PDF)

Inborn errors of metabolism: iron

British medical bulletin, 1999, Vol.55 (3), p.556-567

Worwood, M

1999

Volltextzugriff (PDF)

Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload

Hepatology (Baltimore, Md.), 1998-01, Vol.27 (1), p.289-291

1998

Volltextzugriff (PDF)

What is the role of genetic testing in diagnosis of haemochromatosis?

Annals of clinical biochemistry, 2001-01, Vol.38 (Pt 1), p.3-19

Worwood, M

2001

Volltextzugriff (PDF)

1 – 25 von 340

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(92)
Mit Volltextzugriff
(311)

Publikationsform

Sprache

Englisch
(340)

Erscheinungsjahr

n.n

Thema

Humans
(68)
Science & Technology
(64)
Life Sciences & Biomedicine
(62)
Biological And Medical Sciences
(41)
Medical Sciences
(33)
Hematology
(32)
Hemochromatosis - Genetics
(31)
Female
(28)
Male
(28)
Ferritins - Blood
(21)
Adult
(19)
Hemochromatosis Protein
(19)
Metabolic Diseases
(19)
Histocompatibility Antigens Class I - Genetics
(17)
Mutation
(17)
Other Metabolic Disorders
(16)
Animals
(14)
Middle Aged
(14)
Iron - Metabolism
(13)
Metals
(12)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Erythropoiesis and iron metabolism in dominant erythropoietic protoporphyria

The origin and spread of the HFE-C282Y haemochromatosis mutation

Haptoglobin: a review of the major allele frequencies worldwide and their association with diseases

Co-Inheritance of Mutations in the Uroporphyrinogen Decarboxylase and Hemochromatosis Genes Accelerates the Onset of Porphyria Cutanea Tarda

Serum transferrin receptor assays and their application

Inherited iron loading: genetic testing in diagnosis and management

Iron regulatory protein 1 and 2 in human monocytes, macrophages and duodenum: expression and regulation in hereditary hemochromatosis and iron deficiency

A WHO Reference Reagent for the Serum Transferrin Receptor (sTfR): international collaborative study to evaluate a recombinant soluble transferrin receptor preparation

Soluble transferrin receptor and iron homeostasis

The laboratory assessment of iron status — an update

Diet and genetic factors associated with iron status in middle-aged women

Autosomal dominant reticuloendothelial iron overload associated with a 3–base pair deletion in the ferroportin 1 gene(SLC11A3)

HFE Mutations as risk factors in disease

Automated immunoassay methods for ferritin: recovery studies to assess traceability to an international standard

Hereditary hemochromatosis gene (HFE) variants are associated with birth weight and childhood leukemia risk

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

Headache as a presenting symptom in hereditary hemachromatosis [corrected]

The limited value of methylmalonic acid, homocysteine and holotranscobalamin in the diagnosis of early B12 deficiency

HFE mutations as risk factors in disease: Iron metabolism

HFE gene mutations in susceptibility to childhood leukemia: HuGE review

Hereditary haemochromatosis: only 1% of adult HFE C282Y homozygotes in South Wales have a clinical diagnosis of iron overload

Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis

Inborn errors of metabolism: iron

Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload

What is the role of genetic testing in diagnosis of haemochromatosis?

Suchergebnisse filtern