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...

High mobility group protein B1: a new biomarker of obesity in pregnant women?

Gynecological endocrinology, 2015-02, Vol.31 (2), p.113-115

2015

Volltextzugriff (PDF)

Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens–Johnson syndrome

European archives of paediatric dentistry, 2013-10, Vol.14 (5), p.355-358

2013

Volltextzugriff (PDF)

Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasis

Journal of medical genetics, 2002-09, Vol.39 (9), p.671-675

2002

Volltextzugriff (PDF)

Cadmium concentration in maternal and cord blood and infant birth weight: a study on healthy non-smoking women

Journal of perinatal medicine, 2002-01, Vol.30 (5), p.395-399

2002

Volltextzugriff (PDF)

Monocyte and neutrophil activity after minor surgical stress

Journal of pediatric surgery, 2002-05, Vol.37 (5), p.741-744

2002

Volltextzugriff (PDF)

A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1

European journal of human genetics : EJHG, 2003-06, Vol.11 (6), p.433-436

2003

Volltextzugriff (PDF)

Molecular analysis of sequence variants in the Fcε receptor Iβ gene and IL-4 gene promoter in Italian atopic families

Allergy (Copenhagen), 2004-02, Vol.59 (2), p.213-218

2004

Volltextzugriff (PDF)

Linear scleroderma 'en coup de sabre' associated with facial atrophy in a patient seropositive for Borrelia burgdorferi: a true case of molecular mimicry?

Pediatric allergy and immunology, 2004-12, Vol.15 (6), p.570-572

2004

Volltextzugriff (PDF)

Preliminary data suggest that mutations in the CgRP pathway are not involved in human sporadic cryptorchidism

Journal of endocrinological investigation, 2004-09, Vol.27 (8), p.760-764

2004

Volltextzugriff (PDF)

Allelic association of gene markers on chromosome 11q in Italian families with atopy

Acta Paediatrica, 2000-09, Vol.89 (9), p.1056-1061

2000

Volltextzugriff (PDF)

Genetic basis of non syndromic hypodontia: a DNA investigation performed on three couples of monozygotic twins about PAX9 mutation

European journal of paediatric dentistry, 2011-03, Vol.12 (1), p.21

2011

Volltextzugriff (PDF)

Protein carbonyl group content in patients affected by familiar chronic nail candidiasis

Mediators of Inflammation, 2003-08, Vol.2003 (4), p.247-249

2003

Volltextzugriff (PDF)

Serum levels of malondialdehyde and 4-hydroxy-2,3-nonenal in patients affected by familial chronic nail candidiasis

Inflammation research, 2004-11, Vol.53 (11), p.601-603

2004

Volltextzugriff (PDF)

Epidemiology and Treatment of Otitis Media with Effusion in Children in the First Year of Primary School

Acta oto-laryngologica, 1998, Vol.118 (4), p.557-562

1998

Volltextzugriff (PDF)

Serum Levels of Interleukin-18 in Splenectomized and Nonsplenectomized Thalassemic Patients: Preliminary Considerations

Acta haematologica, 2003-01, Vol.110 (1), p.45-47

2003

Volltextzugriff (PDF)

Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus

Acta diabetologica, 1999-09, Vol.36 (3), p.163-167

1999

Volltextzugriff (PDF)

Reduced plasma c-AMP levels in children with atopic dermatitis

Pediatric allergy and immunology, 1998-08, Vol.9 (3), p.130-132

1998

Volltextzugriff (PDF)

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1074-1078

2013

Volltextzugriff (PDF)

Pain in neonatal intensive care: role of melatonin as an analgesic antioxidant

Journal of pineal research, 2012-04, Vol.52 (3), p.291-295

2012

Volltextzugriff (PDF)

Confirmation of Nablus mask-like facial syndrome

American journal of medical genetics, 2003-09, Vol.121A (3), p.283-285

2003

Volltextzugriff (PDF)

Hallerman-Streiff syndrome: Patient with decreased GH and insulin-like growth factor-1

American journal of medical genetics, 2004-03, Vol.125A (2), p.216-218

2004

Volltextzugriff (PDF)

Molecular analysis of β-thalassaemia patients in a high incidence area of southern Italy

Clinical and laboratory haematology, 2001-12, Vol.23 (6), p.373-378

2001

Volltextzugriff (PDF)

Distinguishing the four genetic causes of jouberts syndrome-related disorders

Annals of neurology, 2005-04, Vol.57 (4), p.513-519

2005

Volltextzugriff (PDF)

Tolerance and pharmacokinetics of ciprofloxacin in the chick. Preliminary experience in subjects of pediatric age with urinary tract infections (UTI)

Research communications in molecular pathology and pharmacology, 1998-02, Vol.99 (2), p.187

1998

Volltextzugriff (PDF)

Description, Nomenclature, and Mapping of a Novel Cerebello-Renal Syndrome with the Molar Tooth Malformation

American journal of human genetics, 2003-09, Vol.73 (3), p.663-670

2003

Volltextzugriff (PDF)

1 – 25 von 186

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(173)
Mit Volltextzugriff
(160)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

High mobility group protein B1: a new biomarker of obesity in pregnant women?

Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens–Johnson syndrome

Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasis

Cadmium concentration in maternal and cord blood and infant birth weight: a study on healthy non-smoking women

Monocyte and neutrophil activity after minor surgical stress

A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1

Molecular analysis of sequence variants in the Fcε receptor Iβ gene and IL-4 gene promoter in Italian atopic families

Linear scleroderma 'en coup de sabre' associated with facial atrophy in a patient seropositive for Borrelia burgdorferi: a true case of molecular mimicry?

Preliminary data suggest that mutations in the CgRP pathway are not involved in human sporadic cryptorchidism

Allelic association of gene markers on chromosome 11q in Italian families with atopy

Genetic basis of non syndromic hypodontia: a DNA investigation performed on three couples of monozygotic twins about PAX9 mutation

Protein carbonyl group content in patients affected by familiar chronic nail candidiasis

Serum levels of malondialdehyde and 4-hydroxy-2,3-nonenal in patients affected by familial chronic nail candidiasis

Epidemiology and Treatment of Otitis Media with Effusion in Children in the First Year of Primary School

Serum Levels of Interleukin-18 in Splenectomized and Nonsplenectomized Thalassemic Patients: Preliminary Considerations

Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus

Reduced plasma c-AMP levels in children with atopic dermatitis

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

Pain in neonatal intensive care: role of melatonin as an analgesic antioxidant

Confirmation of Nablus mask-like facial syndrome

Hallerman-Streiff syndrome: Patient with decreased GH and insulin-like growth factor-1

Molecular analysis of β-thalassaemia patients in a high incidence area of southern Italy

Distinguishing the four genetic causes of jouberts syndrome-related disorders

Tolerance and pharmacokinetics of ciprofloxacin in the chick. Preliminary experience in subjects of pediatric age with urinary tract infections (UTI)

Description, Nomenclature, and Mapping of a Novel Cerebello-Renal Syndrome with the Molar Tooth Malformation

Suchergebnisse filtern