UB Paderborn / Katalog / Suche / in CDI

26 – 50 von 94

Sortiert nach

Perspectives on the Search for a True Physiologic Replacement Therapy for Hypoparathyroidism

European Endocrinology, 2016-03, Vol.12 (1), p.47-48

Winer, Karen K

2016

Link zum Volltext

Verfügbarkeit prüfen

Long-Term Treatment of Hypoparathyroidism: A Randomized Controlled Study Comparing Parathyroid Hormone-(1–34) Versus Calcitriol and Calcium

The journal of clinical endocrinology and metabolism, 2003-09, Vol.88 (9), p.4214-4220

2003

Link zum Volltext

Verfügbarkeit prüfen

Clinical Vignette: PTH(1–34) Replacement Therapy in a Child With Hypoparathyroidism Caused by a Sporadic Calcium Receptor Mutation

Journal of bone and mineral research, 2009-05, Vol.24 (5), p.964-973

2009

Link zum Volltext

Verfügbarkeit prüfen

PTH(1-34) Replacement Therapy in a Child With Hypoparathyroidism Caused by a Sporadic Calcium Receptor Mutation

Journal of bone and mineral research, 2009-05, Vol.24 (5), p.964-973

2009

Link zum Volltext

Verfügbarkeit prüfen

Polyglandular autoimmune syndrome type I - a novel AIRE mutation in a North American patient

Journal of pediatric endocrinology & metabolism : JPEM, 2014-11, Vol.27 (11-12), p.1257

2014

Link zum Volltext

Verfügbarkeit prüfen

Fibroblast Growth Factor‐23 Is Regulated by 1α,25‐Dihydroxyvitamin D

Journal of bone and mineral research, 2005-11, Vol.20 (11), p.1944-1950

2005

Link zum Volltext

Verfügbarkeit prüfen

Forum on aging and skeletal health: Summary of the proceedings of an ASBMR workshop

Journal of bone and mineral research, 2011-11, Vol.26 (11), p.2565-2578

2011

Link zum Volltext

Verfügbarkeit prüfen

Correction: Hypoparathyroidism

Nature reviews. Disease primers, 2017-10, Vol.3 (1), Article 17080

2017

Link zum Volltext

Verfügbarkeit prüfen

A puzzling case of anemia

Transfusion, 2002-12, Vol.42 (12), p.1610-1613

2002

Link zum Volltext

Verfügbarkeit prüfen

Initiation of Continuous rhPTH Infusion With Insulin Pump in an Inpatient Setting

JCEM case reports, 2023-11, Vol.1 (6)

2023

Link zum Volltext

Verfügbarkeit prüfen

Long-term Parathyroid Hormone 1-34 Replacement Therapy inChildren with Hypoparathyroidism

The Journal of pediatrics, 2018-12, Vol.203, p.391-399.e1

2018

Link zum Volltext

Verfügbarkeit prüfen

Prevention of Hypoglycemia During Exercise in Children With Type 1 Diabetes by Suspending Basal Insulin

Diabetes care, 2006-10, Vol.29 (10), p.2200-2204

2006

Link zum Volltext

Verfügbarkeit prüfen

Blunted glucagon but not epinephrine responses to hypoglycemia occurs in youth with less than 1 yr duration of type 1 diabetes mellitus

Pediatric diabetes, 2014-03, Vol.15 (2), p.127-134

2014

Link zum Volltext

Verfügbarkeit prüfen

Achievement of Target A1C Levels With Negligible Hypoglycemia and Low Glucose Variability in Youth With Short-Term Type 1 Diabetes and Residual β-Cell Function

Diabetes care, 2012-04, Vol.35 (4), p.817-820

2012

Link zum Volltext

Verfügbarkeit prüfen

Longitudinal Tracking of DXA Bone Measures Over 6 Years in Children and Adolescents: Persistence of Low Bone Mass to Maturity

The Journal of pediatrics, 2014-01, Vol.164 (6), p.1280-1285.e2

2014

Link zum Volltext

Verfügbarkeit prüfen

A randomized, cross-over trial of once-daily versus twice-daily parathyroid hormone 1-34 in treatment of hypoparathyroidism

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3480-3486

1998

Link zum Volltext

Verfügbarkeit prüfen

Racial Disparity in Fracture Risk Between White and Non-White Children in the United States

The Journal of pediatrics, 2012-09, Vol.161 (6), p.1035-1040.e2

2012

Link zum Volltext

Verfügbarkeit prüfen

Use of the DirecNet Applied Treatment Algorithm (DATA) for diabetes management with a real-time continuous glucose monitor (the FreeStyle Navigator)

Pediatric diabetes, 2008-04, Vol.9 (2), p.142-147

2008

Link zum Volltext

Verfügbarkeit prüfen

Hypoparathyroidism

Nature reviews. Disease primers, 2017-10, Vol.3, p.17080-17080

2017

Link zum Volltext

Verfügbarkeit prüfen

A Randomized, Cross-Over Trial of Once-Daily Versus Twice-Daily Parathyroid Hormone 1–34 in Treatment of Hypoparathyroidism

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3480-3486

1998

Link zum Volltext

Verfügbarkeit prüfen

Hypoparathyroidism

Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism, 2018, p.654-660

2018

Link zum Volltext

Verfügbarkeit prüfen

Comparison of fingerstick hemoglobin A1c levels assayed by DCA 2000 with the DCCT/EDIC central laboratory assay: results of a Diabetes Research in Children Network (DirecNet) Study

Pediatric diabetes, 2005-03, Vol.6 (1), p.13-16

2005

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the Ca2+-Sensing Receptor Gene Cause Autosomal Dominant and Sporadic Hypoparathyroidism

Human molecular genetics, 1996-05, Vol.5 (5), p.601-606

1996

Link zum Volltext

Verfügbarkeit prüfen

A Ca2+-Sensing Receptor Mutation Causes Hypoparathyroidism by Increasing Receptor Sensitivity to Ca2+ and Maximal Signal Transduction1

Pediatric research, 1997-10, Vol.42 (4), p.443-447

1997

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism

Human molecular genetics, 1996-05, Vol.5 (5), p.601-606

1996

Link zum Volltext

Verfügbarkeit prüfen

26 – 50 von 94

Suche als RSS-Feed

Aktive Filter

ThemaChild, Preschool

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(89)
Mit Volltextzugriff
(85)

Publikationsform

Sprache

Englisch
(94)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Perspectives on the Search for a True Physiologic Replacement Therapy for Hypoparathyroidism

Long-Term Treatment of Hypoparathyroidism: A Randomized Controlled Study Comparing Parathyroid Hormone-(1–34) Versus Calcitriol and Calcium

Clinical Vignette: PTH(1–34) Replacement Therapy in a Child With Hypoparathyroidism Caused by a Sporadic Calcium Receptor Mutation

PTH(1-34) Replacement Therapy in a Child With Hypoparathyroidism Caused by a Sporadic Calcium Receptor Mutation

Polyglandular autoimmune syndrome type I - a novel AIRE mutation in a North American patient

Fibroblast Growth Factor‐23 Is Regulated by 1α,25‐Dihydroxyvitamin D

Forum on aging and skeletal health: Summary of the proceedings of an ASBMR workshop

Correction: Hypoparathyroidism

A puzzling case of anemia

Initiation of Continuous rhPTH Infusion With Insulin Pump in an Inpatient Setting

Long-term Parathyroid Hormone 1-34 Replacement Therapy inChildren with Hypoparathyroidism

Prevention of Hypoglycemia During Exercise in Children With Type 1 Diabetes by Suspending Basal Insulin

Blunted glucagon but not epinephrine responses to hypoglycemia occurs in youth with less than 1 yr duration of type 1 diabetes mellitus

Achievement of Target A1C Levels With Negligible Hypoglycemia and Low Glucose Variability in Youth With Short-Term Type 1 Diabetes and Residual β-Cell Function

Longitudinal Tracking of DXA Bone Measures Over 6 Years in Children and Adolescents: Persistence of Low Bone Mass to Maturity

A randomized, cross-over trial of once-daily versus twice-daily parathyroid hormone 1-34 in treatment of hypoparathyroidism

Racial Disparity in Fracture Risk Between White and Non-White Children in the United States

Use of the DirecNet Applied Treatment Algorithm (DATA) for diabetes management with a real-time continuous glucose monitor (the FreeStyle Navigator)

Hypoparathyroidism

A Randomized, Cross-Over Trial of Once-Daily Versus Twice-Daily Parathyroid Hormone 1–34 in Treatment of Hypoparathyroidism

Hypoparathyroidism

Comparison of fingerstick hemoglobin A1c levels assayed by DCA 2000 with the DCCT/EDIC central laboratory assay: results of a Diabetes Research in Children Network (DirecNet) Study

Mutations in the Ca2+-Sensing Receptor Gene Cause Autosomal Dominant and Sporadic Hypoparathyroidism

A Ca2+-Sensing Receptor Mutation Causes Hypoparathyroidism by Increasing Receptor Sensitivity to Ca2+ and Maximal Signal Transduction1

Mutations in the Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism

Aktive Filter

Suchergebnisse filtern