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...

Bipolar membrane electrodialysis for mixed salt water treatment: determination of optimum conditions by topsis-based taguchi method

International journal of environmental science and technology (Tehran), 2023, Vol.20 (1), p.587-604

2023

Volltextzugriff (PDF)

A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3448-3451

2001

Volltextzugriff (PDF)

Hypovolemia-related gastric tissue damage in the setting of upper gastrointestinal bleeding

The Turkish journal of gastroenterology, 2010-03, Vol.21 (1), p.17-22

2010

Volltextzugriff (PDF)

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey

Haematologica (Roma), 2000-03, Vol.85 (3), p.320

2000

Volltextzugriff (PDF)

Evaluation of the functional and radiologic outcomes in talus fractures following surgery

European review for medical and pharmacological sciences, 2024-04, Vol.28 (8), p.3176

2024

Volltextzugriff (PDF)

Transfusion-Associated Graft-versus-Host Disease in Patients with and without Immunodeficiency: Report of Six Cases

Transfusion medicine and hemotherapy, 2007-01, Vol.34 (1), p.79-82

2007

Volltextzugriff (PDF)

The molecular basis of familial hypercholesterolaemia in Turkish patients

Atherosclerosis, 2005-05, Vol.180 (1), p.63-71

2005

Volltextzugriff (PDF)

A new Turkish type of β‐thalassaemia major with homozygosity for two non‐consecutive 7.6 kb deletions of the Ψβ and β genes and an intact δ gene

British journal of haematology, 1995-02, Vol.89 (2), p.306-312

1995

Volltextzugriff (PDF)

Molecular Analysis of Turkish β-Thalassemia Heterozygotes with Normal Hb A2 Levels

Hemoglobin, 2000, Vol.24 (3), p.195-201

2000

Volltextzugriff (PDF)

Evaluation of Three Different Posts in The Restoration of Severely Decayed Primary Maxillary Anterior Teeth: A 24-Month Clinical Study

Oral Health and Dental science, 2020-03, Vol.4 (1)

2020

Volltextzugriff (PDF)

Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene

British journal of haematology, 1991-10, Vol.79 (2), p.306-310

1991

Volltextzugriff (PDF)

Hydrofluoric acid and sodium hydroxide production by bipolar membrane electrodialysis

Desalination and water treatment, 2016-09, Vol.57 (43), p.20254-20260

2016

Volltextzugriff (PDF)

Mitochondrial DNA sequence variation in the Anatolian Peninsula (Turkey)

Journal of genetics, 2004-04, Vol.83 (1), p.39-47

2004

Volltextzugriff (PDF)

Cytomegalovirus Antibody Titers in Patients with Bechet's Disease

Internal medicine open access, 2018, Vol.8 (1)

2018

Volltextzugriff (PDF)

Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family

American journal of hematology, 2004-08, Vol.76 (4), p.378-382

2004

Volltextzugriff (PDF)

βs haplotypes in various world populations

Human genetics, 1992-04, Vol.89 (1), p.99-104

1992

Volltextzugriff (PDF)

β‐Thalassaemia intermedia in a Turkish girl: homozygosity for G→A substitution at +22 relative to the β‐globin cap site

British journal of haematology, 2001-10, Vol.115 (1), p.90-94

2001

Volltextzugriff (PDF)

Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion

British journal of haematology, 2002-07, Vol.118 (1), p.278-281

2002

Volltextzugriff (PDF)

AOSpine Masters Series, Volume 5: Cervical Spine Trauma

Luiz Roberto Gomes Vialle / F. Cumhur Oner, Alexander R. Vaccaro

2015

Volltextzugriff (PDF)

The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene

Blood, 1991-03, Vol.77 (5), p.1124-1125

1991

Volltextzugriff (PDF)

(beta)-thalassaemia intermedia in a Turkish girl: Homozygosity for G-->A substitution at +22 relative to the (beta)-globin cap site

British journal of haematology, 2001-10, Vol.115 (1), p.90

2001

Volltextzugriff (PDF)

Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients

European journal of haematology, 2003-07, Vol.71 (1), p.39-43

2003

Volltextzugriff (PDF)

Coexistence of Hb Lepore-Boston-Washington (δ87GLN-β-IVS-II-8) With α-Thalassemia [α(-5NT)α/αα]

Hemoglobin, 1998-01, Vol.22 (3), p.273-276

1998

Volltextzugriff (PDF)

CHRONIC HEMOLYTIC ANEMIA ASSOCIATED WITH GLUCOSE 6-PHOSPHATE DEHYDROGENASE (GUADALAJARA)1159 C → T (387 ARG → CYS) DEFICIENCY ASSOCIATED WITH GILBERT SYNDROME IN A TURKISH PATIENT

Pediatric hematology and oncology, 2002, Vol.19 (1), p.39-44

2002

Volltextzugriff (PDF)

Effects of neutral, cationic, and anionic chromium ascorbate complexes on isolated human mitochondrial and genomic DNA

BMB reports, 2003-07, Vol.36 (4), p.403-408

2003

Volltextzugriff (PDF)

1 – 25 von 524

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(458)
Mit Volltextzugriff
(392)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(510)
Deutsch
(5)
Serbian
(1)
Türkisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Bipolar membrane electrodialysis for mixed salt water treatment: determination of optimum conditions by topsis-based taguchi method

A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity

Hypovolemia-related gastric tissue damage in the setting of upper gastrointestinal bleeding

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey

Evaluation of the functional and radiologic outcomes in talus fractures following surgery

Transfusion-Associated Graft-versus-Host Disease in Patients with and without Immunodeficiency: Report of Six Cases

The molecular basis of familial hypercholesterolaemia in Turkish patients

A new Turkish type of β‐thalassaemia major with homozygosity for two non‐consecutive 7.6 kb deletions of the Ψβ and β genes and an intact δ gene

Molecular Analysis of Turkish β-Thalassemia Heterozygotes with Normal Hb A2 Levels

Evaluation of Three Different Posts in The Restoration of Severely Decayed Primary Maxillary Anterior Teeth: A 24-Month Clinical Study

Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene

Hydrofluoric acid and sodium hydroxide production by bipolar membrane electrodialysis

Mitochondrial DNA sequence variation in the Anatolian Peninsula (Turkey)

Cytomegalovirus Antibody Titers in Patients with Bechet's Disease

Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family

βs haplotypes in various world populations

β‐Thalassaemia intermedia in a Turkish girl: homozygosity for G→A substitution at +22 relative to the β‐globin cap site

Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion

AOSpine Masters Series, Volume 5: Cervical Spine Trauma

The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene

(beta)-thalassaemia intermedia in a Turkish girl: Homozygosity for G-->A substitution at +22 relative to the (beta)-globin cap site

Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients

Coexistence of Hb Lepore-Boston-Washington (δ87GLN-β-IVS-II-8) With α-Thalassemia [α(-5NT)α/αα]

CHRONIC HEMOLYTIC ANEMIA ASSOCIATED WITH GLUCOSE 6-PHOSPHATE DEHYDROGENASE (GUADALAJARA)1159 C → T (387 ARG → CYS) DEFICIENCY ASSOCIATED WITH GILBERT SYNDROME IN A TURKISH PATIENT

Effects of neutral, cationic, and anionic chromium ascorbate complexes on isolated human mitochondrial and genomic DNA

Suchergebnisse filtern