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Gabriele Haeusler

Showing results (21-30 of 29) with videos related to

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Frontiers in Endocrinology|April 11, 2022
Persistent Lower Limb Deformities Despite Amelioration of Rickets in X-Linked Hypophosphatemia (XLH) - A Prospective Observational StudyGabriel T Mindler, Alexandra Stauffer, Andreas Kranzl, et al.
Plos One|October 23, 2013
Insulin-like growth factor I (IGF-1) Ec/Mechano Growth factor--a splice variant of IGF-1 within the growth plateWerner Schlegel, Adalbert Raimann, Daniel Halbauer, et al.
Hormone Research in Paediatrics|October 21, 2021
Lethal Encephalopathy in an Infant with Hypophosphatasia despite Enzyme Replacement TherapyAdalbert Raimann, Christine Haberler, Janina Patsch, et al.
The Journal of Clinical Endocrinology and Metabolism|April 5, 2007
Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous statesPeng Fang, Stefan Riedl, Serge Amselem, et al.
Nature Communications|February 5, 2022
A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorderJulian C Lui, Adalbert Raimann, Hironori Hojo, et al.
Orphanet Journal of Rare Diseases|November 12, 2022
Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormoneDiana-Alexandra Ertl, Justin Le Lorier, Andreas Gleiss, et al.
Journal of Structural Biology|July 4, 2020
Alterations of bone material properties in adult patients with X-linked hypophosphatemia (XLH)Nadja Fratzl-Zelman, Sonja Gamsjaeger, Stéphane Blouin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2010
Impact of heterozygosity for acid-labile subunit (IGFALS) gene mutations on stature: results from the international acid-labile subunit consortiumOlga V Fofanova-Gambetti, Vivian Hwa, Jan M Wit, et al.
Orphanet Journal of Rare Diseases|March 16, 2023
Lifetime impact of achondroplasia study in Europe (LIAISE): findings from a multinational observational studyMohamad Maghnie, Oliver Semler, Encarna Guillen-Navarro, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Frontiers in Endocrinology|April 11, 2022
Persistent Lower Limb Deformities Despite Amelioration of Rickets in X-Linked Hypophosphatemia (XLH) - A Prospective Observational StudyGabriel T Mindler, Alexandra Stauffer, Andreas Kranzl, et al.
Plos One|October 23, 2013
Insulin-like growth factor I (IGF-1) Ec/Mechano Growth factor--a splice variant of IGF-1 within the growth plateWerner Schlegel, Adalbert Raimann, Daniel Halbauer, et al.
Hormone Research in Paediatrics|October 21, 2021
Lethal Encephalopathy in an Infant with Hypophosphatasia despite Enzyme Replacement TherapyAdalbert Raimann, Christine Haberler, Janina Patsch, et al.
The Journal of Clinical Endocrinology and Metabolism|April 5, 2007
Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous statesPeng Fang, Stefan Riedl, Serge Amselem, et al.
Nature Communications|February 5, 2022
A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorderJulian C Lui, Adalbert Raimann, Hironori Hojo, et al.
Orphanet Journal of Rare Diseases|November 12, 2022
Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormoneDiana-Alexandra Ertl, Justin Le Lorier, Andreas Gleiss, et al.
Journal of Structural Biology|July 4, 2020
Alterations of bone material properties in adult patients with X-linked hypophosphatemia (XLH)Nadja Fratzl-Zelman, Sonja Gamsjaeger, Stéphane Blouin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2010
Impact of heterozygosity for acid-labile subunit (IGFALS) gene mutations on stature: results from the international acid-labile subunit consortiumOlga V Fofanova-Gambetti, Vivian Hwa, Jan M Wit, et al.
Orphanet Journal of Rare Diseases|March 16, 2023
Lifetime impact of achondroplasia study in Europe (LIAISE): findings from a multinational observational studyMohamad Maghnie, Oliver Semler, Encarna Guillen-Navarro, et al.
Pageof 3