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...

Hypophosphatasia: Enzyme Replacement Therapy Brings New Opportunities and New Challenges

Journal of bone and mineral research, 2017-04, Vol.32 (4), p.667-675

Whyte, Michael P

2017

Volltextzugriff (PDF)

Physiological role of alkaline phosphatase explored in hypophosphatasia

Annals of the New York Academy of Sciences, 2010-04, Vol.1192 (1), p.190-200

Whyte, Michael P.

2010

Volltextzugriff (PDF)

Skeletal and extraskeletal disorders of biomineralization

Nature reviews. Endocrinology, 2022-08, Vol.18 (8), p.473-489

2022

Volltextzugriff (PDF)

Hypophosphatasia: Natural history study of 101 affected children investigated at one research center

Bone (New York, N.Y.), 2016-12, Vol.93, p.125-138

2016

Volltextzugriff (PDF)

Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment

Nature reviews. Endocrinology, 2016-04, Vol.12 (4), p.233-246

Whyte, Michael P

2016

Volltextzugriff (PDF)

Atypical Femoral Fractures, Bisphosphonates, and Adult Hypophosphatasia

Journal of bone and mineral research, 2009-06, Vol.24 (6), p.1132-1134

Whyte, Michael P

2009

Volltextzugriff (PDF)

Hypophosphatasia: An overview For 2017

Bone (New York, N.Y.), 2017-09, Vol.102, p.15-25

Whyte, Michael P

2017

Volltextzugriff (PDF)

Atypical Subtrochanteric and Diaphyseal Femoral Fractures: Second Report of a Task Force of the American Society for Bone and Mineral Research

Journal of bone and mineral research, 2014-01, Vol.29 (1), p.1-23

2014

Volltextzugriff (PDF)

“Atypical femoral fractures” during bisphosphonate exposure in adult hypophosphatasia

Journal of bone and mineral research, 2012-05, Vol.27 (5), p.987-994

2012

Volltextzugriff (PDF)

Validation of a Novel Scoring System for Changes in Skeletal Manifestations of Hypophosphatasia in Newborns, Infants, and Children: The Radiographic Global Impression of Change Scale

Journal of bone and mineral research, 2018-05, Vol.33 (5), p.868-874

2018

Volltextzugriff (PDF)

Natural History of Perinatal and Infantile Hypophosphatasia: A Retrospective Study

The Journal of pediatrics, 2019-06, Vol.209, p.116-124.e4

2019

Volltextzugriff (PDF)

Carbonic anhydrase II deficiency

Bone (New York, N.Y.), 2023-04, Vol.169, p.116684-116684, Article 116684

Whyte, Michael P.

2023

Volltextzugriff (PDF)

Osteopetrosis: Discovery and early history of “marble bone disease”

Bone (New York, N.Y.), 2023-06, Vol.171, p.116737-116737, Article 116737

Whyte, Michael P.

2023

Volltextzugriff (PDF)

AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity

Cell reports (Cambridge), 2018-01, Vol.22 (4), p.1054-1066

2018

Volltextzugriff (PDF)

Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9

Bone (New York, N.Y.), 2016-03, Vol.84, p.289-298

2016

Volltextzugriff (PDF)

Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review)

Journal of bone and mineral research, 2011-10, Vol.26 (10), p.2389-2398

2011

Volltextzugriff (PDF)

Enzyme Replacement Therapy for Murine Hypophosphatasia

Journal of bone and mineral research, 2008-06, Vol.23 (6), p.777-787

2008

Volltextzugriff (PDF)

Author Correction: Skeletal and extraskeletal disorders of biomineralization

Nature reviews. Endocrinology, 2023, Vol.19 (1), p.62-62

2023

Volltextzugriff (PDF)

Calcific Periarthritis as the Only Clinical Manifestation of Hypophosphatasia in Middle‐Aged Sisters

Journal of bone and mineral research, 2014-04, Vol.29 (4), p.929-934

2014

Volltextzugriff (PDF)

Alkaline Phosphatase and Hypophosphatasia

Calcified tissue international, 2016-04, Vol.98 (4), p.398-416

2016

Volltextzugriff (PDF)

Tumor‐Induced Osteomalacia: Treatment Progress Using Burosumab, an Anti‐FGF23 Monoclonal Antibody

Journal of bone and mineral research, 2021-04, Vol.36 (4), p.625-626

Whyte, Michael P

2021

Volltextzugriff (PDF)

Enzyme replacement prevents enamel defects in hypophosphatasia mice

Journal of bone and mineral research, 2012-08, Vol.27 (8), p.1722-1734

2012

Volltextzugriff (PDF)

Osteopetrosis: Gene-based nosology and significance

Bone (New York, N.Y.), 2023-10, Vol.175, p.116854-116854, Article 116854

2023

Volltextzugriff (PDF)

Alkaline Phosphatase: Discovery and Naming of Our Favorite Enzyme

Journal of bone and mineral research, 2018-02, Vol.33 (2), p.362-364

2018

Volltextzugriff (PDF)

LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low‐Density Lipoprotein Receptor‐Related Protein 6

JBMR plus, 2023-04, Vol.7 (4), p.e10717-n/a

2023

Volltextzugriff (PDF)

1 – 25 von 661

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(434)
Mit Volltextzugriff
(554)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(661)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Hypophosphatasia: Enzyme Replacement Therapy Brings New Opportunities and New Challenges

Physiological role of alkaline phosphatase explored in hypophosphatasia

Skeletal and extraskeletal disorders of biomineralization

Hypophosphatasia: Natural history study of 101 affected children investigated at one research center

Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment

Atypical Femoral Fractures, Bisphosphonates, and Adult Hypophosphatasia

Hypophosphatasia: An overview For 2017

Atypical Subtrochanteric and Diaphyseal Femoral Fractures: Second Report of a Task Force of the American Society for Bone and Mineral Research

“Atypical femoral fractures” during bisphosphonate exposure in adult hypophosphatasia

Validation of a Novel Scoring System for Changes in Skeletal Manifestations of Hypophosphatasia in Newborns, Infants, and Children: The Radiographic Global Impression of Change Scale

Natural History of Perinatal and Infantile Hypophosphatasia: A Retrospective Study

Carbonic anhydrase II deficiency

Osteopetrosis: Discovery and early history of “marble bone disease”

AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity

Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9

Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review)

Enzyme Replacement Therapy for Murine Hypophosphatasia

Author Correction: Skeletal and extraskeletal disorders of biomineralization

Calcific Periarthritis as the Only Clinical Manifestation of Hypophosphatasia in Middle‐Aged Sisters

Alkaline Phosphatase and Hypophosphatasia

Tumor‐Induced Osteomalacia: Treatment Progress Using Burosumab, an Anti‐FGF23 Monoclonal Antibody

Enzyme replacement prevents enamel defects in hypophosphatasia mice

Osteopetrosis: Gene-based nosology and significance

Alkaline Phosphatase: Discovery and Naming of Our Favorite Enzyme

LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low‐Density Lipoprotein Receptor‐Related Protein 6

Suchergebnisse filtern