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...

Nonalcoholic steatohepatitis in Asian Indians is neither associated with iron overload nor with HFE gene mutations

World journal of gastroenterology : WJG, 2005-01, Vol.11 (3), p.393

2005

Volltextzugriff (PDF)

Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India

World journal of gastroenterology : WJG, 2007-06, Vol.13 (21), p.2956

2007

Volltextzugriff (PDF)

Parvovirus B19 infection-associated red-cell aplasia in renal-transplant recipients: clues from the bone marrow

Transplantation, 2004-01, Vol.77 (2), p.320-321

2004

Volltextzugriff (PDF)

Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians

Blood cells, molecules, & diseases, 2018-11, Vol.73, p.14-21

2018

Volltextzugriff (PDF)

Acute leukemia/myelodysplastic syndrome as a sequelae of carcinoma breast: a report of five cases from north India

Indian journal of pathology & microbiology, 2009-04, Vol.52 (2), p.167-170

2009

Volltextzugriff (PDF)

Donor blood glucose 6-phosphate dehydrogenase deficiency reduces the efficacy of exchange transfusion in neonatal hyperbilirubinemia

Pediatrics (Evanston), 2009-01, Vol.123 (1), p.e96-e100

2009

Volltextzugriff (PDF)

The clinical significance of the spectrum of interactions of CAP+1 (A→C), a silent β-globin gene mutation, with other β-thalassemia mutations and globin gene modifiers in north Indians

European journal of haematology, 2007-11, Vol.79 (5), p.417-421

2007

Volltextzugriff (PDF)

Spectrum of β-Thalassemia Mutations in Punjabis

International journal of human genetics, 2003-10, Vol.3 (4)

Garewal, Gurjeewan

2003

Volltextzugriff (PDF)

Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait

European journal of haematology, 2005-04, Vol.74 (4), p.333-336

2005

Volltextzugriff (PDF)

Serum transferrin receptor-ferritin index shows concomitant iron deficiency anemia and anemia of chronic disease is common in patients with rheumatoid arthritis in north India

Indian journal of pathology & microbiology, 2008-01, Vol.51 (1), p.102-104

2008

Volltextzugriff (PDF)

The reticulin stain in bone marrow biopsies – beyond marrow fibrosis

British journal of haematology, 2003-11, Vol.123 (3), p.379-379

2003

Volltextzugriff (PDF)

Antiphospholipid antibodies in children with systemic lupus erythematosus : a prospective study in northern India

Rheumatology international, 2005-09, Vol.25 (7), p.530-535

2005

Volltextzugriff (PDF)

Spectrum of β-Thalassemia Mutations in Punjabis

International journal of human genetics, 2003-12, Vol.3 (4), p.217-219

2003

Volltextzugriff (PDF)

The utility of bone marrow examination in renal transplantation: nine years of experience from north India

Transplantation, 2006-05, Vol.81 (9), p.1354-1356

2006

Volltextzugriff (PDF)

AUTOMATED RETICULOCYTE RESPONSE IS A GOOD PREDICTOR OF BONE-MARROW RECOVERY IN PEDIATRIC MALIGNANCIES

Pediatric hematology and oncology, 2006-06, Vol.23 (4), p.299-305

2006

Volltextzugriff (PDF)

Nucleotide −88 (C‐T) promoter mutation is a common β‐thalassemia mutation in the Jat Sikhs of Punjab, India

American journal of hematology, 2005-08, Vol.79 (4), p.252-256

2005

Volltextzugriff (PDF)

Platelet function disorders

Indian journal of pediatrics, 2003-12, Vol.70 (12), p.983-987

2003

Volltextzugriff (PDF)

Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) in Myelodysplastic Syndrome

Pediatric hematology and oncology, 1993, Vol.10 (4), p.343-346

1993

Volltextzugriff (PDF)

Charcot Leyden crystals in acute myeloid leukemia

American journal of hematology, 2003-06, Vol.73 (2), p.141-141

2003

Volltextzugriff (PDF)

Comparative study of myelodysplastic syndromes and normal bone marrow biopsies with conventional staining and immunocytochemistry

Analytical and quantitative cytology and histology, 2005-06, Vol.27 (3), p.152

2005

Volltextzugriff (PDF)

HEMATOLOGICAL DISORDERS IN DOWN SYNDROME: Ten-Year Experience at a Tertiary Care Centre in North India

Pediatric hematology and oncology, 2005-09, Vol.22 (6), p.507-512

2005

Volltextzugriff (PDF)

INTERFERON THERAPY IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I/II

Pediatric hematology and oncology, 2005-03, Vol.22 (2), p.133-138

2005

Volltextzugriff (PDF)

Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [α 14 (A12) Try → Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease

Hematology (Luxembourg), 2005-10, Vol.10 (5), p.427-429

2005

Volltextzugriff (PDF)

Congenital dyserythropoietic anemia: Clinical and hematological profile

Indian pediatrics, 2003-06, Vol.40 (6), p.551-555

2003

Volltextzugriff (PDF)

Image morphometry of acute leukemias. Comparison between lymphoid and myeloid subtypes

Analytical and quantitative cytology and histology, 2004-02, Vol.26 (1), p.57

2004

Volltextzugriff (PDF)

1 – 25 von 32

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(21)

Publikationsform

Artikel
(31)
Berichte
(1)

Sprache

Englisch
(32)

Erscheinungsjahr

n.n

Thema

Humans
(28)
Life Sciences & Biomedicine
(23)
Science & Technology
(23)
Female
(18)
Male
(18)
Adult
(13)
Hematology
(13)
Middle Aged
(9)
India
(8)
Child
(7)
Adolescent
(6)
Biological And Medical Sciences
(6)
Medical Sciences
(6)
Hematologic And Hematopoietic Diseases
(5)
Heterozygote
(5)
Homozygote
(5)
Infant, Newborn
(5)
Pediatrics
(5)
Aged
(4)
Child, Preschool
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Nonalcoholic steatohepatitis in Asian Indians is neither associated with iron overload nor with HFE gene mutations

Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India

Parvovirus B19 infection-associated red-cell aplasia in renal-transplant recipients: clues from the bone marrow

Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians

Acute leukemia/myelodysplastic syndrome as a sequelae of carcinoma breast: a report of five cases from north India

Donor blood glucose 6-phosphate dehydrogenase deficiency reduces the efficacy of exchange transfusion in neonatal hyperbilirubinemia

The clinical significance of the spectrum of interactions of CAP+1 (A→C), a silent β-globin gene mutation, with other β-thalassemia mutations and globin gene modifiers in north Indians

Spectrum of β-Thalassemia Mutations in Punjabis

Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait

Serum transferrin receptor-ferritin index shows concomitant iron deficiency anemia and anemia of chronic disease is common in patients with rheumatoid arthritis in north India

The reticulin stain in bone marrow biopsies – beyond marrow fibrosis

Antiphospholipid antibodies in children with systemic lupus erythematosus : a prospective study in northern India

Spectrum of β-Thalassemia Mutations in Punjabis

The utility of bone marrow examination in renal transplantation: nine years of experience from north India

AUTOMATED RETICULOCYTE RESPONSE IS A GOOD PREDICTOR OF BONE-MARROW RECOVERY IN PEDIATRIC MALIGNANCIES

Nucleotide −88 (C‐T) promoter mutation is a common β‐thalassemia mutation in the Jat Sikhs of Punjab, India

Platelet function disorders

Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) in Myelodysplastic Syndrome

Charcot Leyden crystals in acute myeloid leukemia

Comparative study of myelodysplastic syndromes and normal bone marrow biopsies with conventional staining and immunocytochemistry

HEMATOLOGICAL DISORDERS IN DOWN SYNDROME: Ten-Year Experience at a Tertiary Care Centre in North India

INTERFERON THERAPY IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I/II

Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [α 14 (A12) Try → Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease

Congenital dyserythropoietic anemia: Clinical and hematological profile

Image morphometry of acute leukemias. Comparison between lymphoid and myeloid subtypes

Suchergebnisse filtern