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...

Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland

PloS one, 2015-07, Vol.10 (7), p.e0131883-e0131883

2015

Volltextzugriff (PDF)

Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults

Journal of bone and mineral research, 2016-09, Vol.31 (9), p.1734-1742

2016

Volltextzugriff (PDF)

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants

Osteoporosis international, 2017-10, Vol.28 (10), p.3023-3032

2017

Volltextzugriff (PDF)

Cartilage‐hair hypoplasia with normal height in childhood—4 patients with a unique genotype

Clinical genetics, 2017-08, Vol.92 (2), p.204-207

2017

Volltextzugriff (PDF)

Bone Characteristics and Their Determinants in Adolescents and Young Adults with Early-Onset Severe Obesity

Calcified tissue international, 2015-10, Vol.97 (4), p.364-375

2015

Volltextzugriff (PDF)

Body composition and adipokines in patients with juvenile idiopathic arthritis and systemic glucocorticoids

Clinical and experimental rheumatology, 2015-11, Vol.33 (6), p.924

2015

Volltextzugriff (PDF)

Impaired Bone Health in Adolescents After Liver Transplantation

American journal of transplantation, 2008-01, Vol.8 (1), p.150-157

2008

Volltextzugriff (PDF)

Hypercalciuria and kidney function in children with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-03, Vol.19 (2), p.200-205

2013

Volltextzugriff (PDF)

Compromised Peak Bone Mass in Patients with Inflammatory Bowel Disease–A Prospective Study

The Journal of pediatrics, 2014-06, Vol.164 (6), p.1436-1443.e1

2014

Volltextzugriff (PDF)

Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort

Prenatal diagnosis, 2022-11, Vol.42 (12), p.1525-1537

2022

Volltextzugriff (PDF)

Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss‐of‐Function Gα11 Mutation

Journal of bone and mineral research, 2018-01, Vol.33 (1), p.32-41

2018

Volltextzugriff (PDF)

Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia

Frontiers in genetics, 2021-06, Vol.12, p.680838-680838

2021

Volltextzugriff (PDF)

Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia

Journal of allergy and clinical immunology, 2017-08, Vol.140 (2), p.612-614.e5

2017

Volltextzugriff (PDF)

Fatigue and disturbances of sleep in patients with osteogenesis imperfecta - a cross-sectional questionnaire study

BMC musculoskeletal disorders, 2018-01, Vol.19 (1), p.3-3, Article 3

2018

Volltextzugriff (PDF)

Timing of dental development in osteogenesis imperfecta patients with and without bisphosphonate treatment

Bone (New York, N.Y.), 2017-01, Vol.94, p.29-33

2017

Volltextzugriff (PDF)

Scoliosis After Solid Organ Transplantation in Children and Adolescents

American journal of transplantation, 2006-02, Vol.6 (2), p.324-330

2006

Volltextzugriff (PDF)

Positive airway pressure therapy for obstructive sleep apnea in patients with Osteogenesis imperfecta: a prospective pilot study

BMC musculoskeletal disorders, 2021-01, Vol.22 (1), p.61-61, Article 61

2021

Volltextzugriff (PDF)

High prevalence of asymptomatic vertebral fractures in children after orthotopic liver transplantation

Bone (New York, N.Y.), 2007-06, Vol.40 (6), p.S82-S83

2007

Volltextzugriff (PDF)

Bisphosphonate Treatment and the Characteristics of Femoral Fractures in Children With Osteogenesis Imperfecta

The journal of clinical endocrinology and metabolism, 2017-04, Vol.102 (4), p.1333-1339

2017

Volltextzugriff (PDF)

Impaired Bone Health in Inflammatory Bowel Disease: A Case–Control Study in 80 Pediatric Patients

Calcified tissue international, 2012-08, Vol.91 (2), p.121-130

2012

Volltextzugriff (PDF)

Is sleep apnea underdiagnosed in adult patients with osteogenesis imperfecta? -a single-center cross-sectional study

Orphanet journal of rare diseases, 2018-12, Vol.13 (1), p.231-231, Article 231

2018

Volltextzugriff (PDF)

Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia

Journal of bone and mineral research, 2021-02, Vol.36 (2), p.283-297

2021

Volltextzugriff (PDF)

A Wide Spectrum of Autoimmune Manifestations and Other Symptoms Suggesting Immune Dysregulation in Patients With Cartilage-Hair Hypoplasia

Frontiers in immunology, 2018-10, Vol.9, p.2468-2468

2018

Volltextzugriff (PDF)

Altered Osteocyte-Specific Protein Expression in Bone after Childhood Solid Organ Transplantation

PloS one, 2015-09, Vol.10 (9), p.e0138156-e0138156

2015

Volltextzugriff (PDF)

Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux

European journal of medical genetics, 2019-09, Vol.62 (9), p.103554-103554, Article 103554

2019

Volltextzugriff (PDF)

1 – 25 von 84

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(78)
Mit Volltextzugriff
(77)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland

Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants

Cartilage‐hair hypoplasia with normal height in childhood—4 patients with a unique genotype

Bone Characteristics and Their Determinants in Adolescents and Young Adults with Early-Onset Severe Obesity

Body composition and adipokines in patients with juvenile idiopathic arthritis and systemic glucocorticoids

Impaired Bone Health in Adolescents After Liver Transplantation

Hypercalciuria and kidney function in children with haemophilia

Compromised Peak Bone Mass in Patients with Inflammatory Bowel Disease–A Prospective Study

Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort

Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss‐of‐Function Gα11 Mutation

Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia

Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia

Fatigue and disturbances of sleep in patients with osteogenesis imperfecta - a cross-sectional questionnaire study

Timing of dental development in osteogenesis imperfecta patients with and without bisphosphonate treatment

Scoliosis After Solid Organ Transplantation in Children and Adolescents

Positive airway pressure therapy for obstructive sleep apnea in patients with Osteogenesis imperfecta: a prospective pilot study

High prevalence of asymptomatic vertebral fractures in children after orthotopic liver transplantation

Bisphosphonate Treatment and the Characteristics of Femoral Fractures in Children With Osteogenesis Imperfecta

Impaired Bone Health in Inflammatory Bowel Disease: A Case–Control Study in 80 Pediatric Patients

Is sleep apnea underdiagnosed in adult patients with osteogenesis imperfecta? -a single-center cross-sectional study

Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia

A Wide Spectrum of Autoimmune Manifestations and Other Symptoms Suggesting Immune Dysregulation in Patients With Cartilage-Hair Hypoplasia

Altered Osteocyte-Specific Protein Expression in Bone after Childhood Solid Organ Transplantation

Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux

Suchergebnisse filtern