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Lothar Seefried

Showing results (61-70 of 73) with videos related to

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European Cells & Materials|December 15, 2010
A small scale cell culture system to analyze mechanobiology using reporter gene constructs and polyurethane dishesLothar Seefried, Sigrid Mueller-Deubert, Thomas Schwarz, et al.
Molecular Genetics and Metabolism|September 11, 2017
Monitoring guidance for patients with hypophosphatasia treated with asfotase alfaPriya S Kishnani, Eric T Rush, Paul Arundel, et al.
Orphanet Journal of Rare Diseases|November 25, 2025
The Global Hypophosphatasia Registry: lessons learned from a decade of real-world dataPriya S Kishnani, Lothar Seefried, Keiichi Ozono, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2022
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass DisordersRalf Oheim, Elena Tsourdi, Lothar Seefried, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 3, 2025
Biochemical phenotype of hypophosphatasia in asymptomatic individuals carrying ALPL variantsRodrigo Montero-Lopez, Mariam R Farman, Florian Högler, et al.
Nature Reviews. Nephrology|January 15, 2025
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemiaDieter Haffner, Francesco Emma, Lothar Seefried, et al.
Bone|October 28, 2023
The Global ALPL gene variant classification project: Dedicated to deciphering variantsMariam R Farman, Catherine Rehder, Theodora Malli, et al.
JBMR Plus|May 19, 2025
The ALPL gene variant project: results of the first 100 reclassified variantsMariam R Farman, Theodora Malli, Catherine Rehder, et al.
Calcified Tissue International|May 2, 2025
Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright SyndromeAna Luisa Priego Zurita, Oana O Bulaicon, Jillian Bryce, et al.
Nature Reviews. Endocrinology|April 28, 2022
Interdisciplinary management of FGF23-related phosphate wasting syndromes: a Consensus Statement on the evaluation, diagnosis and care of patients with X-linked hypophosphataemiaAndrea Trombetti, Nasser Al-Daghri, Maria Luisa Brandi, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
European Cells & Materials|December 15, 2010
A small scale cell culture system to analyze mechanobiology using reporter gene constructs and polyurethane dishesLothar Seefried, Sigrid Mueller-Deubert, Thomas Schwarz, et al.
Molecular Genetics and Metabolism|September 11, 2017
Monitoring guidance for patients with hypophosphatasia treated with asfotase alfaPriya S Kishnani, Eric T Rush, Paul Arundel, et al.
Orphanet Journal of Rare Diseases|November 25, 2025
The Global Hypophosphatasia Registry: lessons learned from a decade of real-world dataPriya S Kishnani, Lothar Seefried, Keiichi Ozono, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2022
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass DisordersRalf Oheim, Elena Tsourdi, Lothar Seefried, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 3, 2025
Biochemical phenotype of hypophosphatasia in asymptomatic individuals carrying ALPL variantsRodrigo Montero-Lopez, Mariam R Farman, Florian Högler, et al.
Nature Reviews. Nephrology|January 15, 2025
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemiaDieter Haffner, Francesco Emma, Lothar Seefried, et al.
Bone|October 28, 2023
The Global ALPL gene variant classification project: Dedicated to deciphering variantsMariam R Farman, Catherine Rehder, Theodora Malli, et al.
JBMR Plus|May 19, 2025
The ALPL gene variant project: results of the first 100 reclassified variantsMariam R Farman, Theodora Malli, Catherine Rehder, et al.
Calcified Tissue International|May 2, 2025
Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright SyndromeAna Luisa Priego Zurita, Oana O Bulaicon, Jillian Bryce, et al.
Nature Reviews. Endocrinology|April 28, 2022
Interdisciplinary management of FGF23-related phosphate wasting syndromes: a Consensus Statement on the evaluation, diagnosis and care of patients with X-linked hypophosphataemiaAndrea Trombetti, Nasser Al-Daghri, Maria Luisa Brandi, et al.
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