Search research articles
Contact Us
Filters
Showing results (51-60 of 77) with videos related to
Page
of 8
Sort By:
Plos One
|
October 27, 2017
Lower incidence of fracture after IV bisphosphonates in girls with Rett syndrome and severe bone fragility
Anne-Sophie Lambert, Anya Rothenbuhler, Perrine Charles, et al.
European Journal of Endocrinology
|
December 3, 2020
Inactivating PTH/PTHrP signaling disorders (iPPSDs): evaluation of the new classification in a multicenter large series of 544 molecularly characterized patients
Arrate Pereda, Francesca M Elli, Suzanne Thiele, et al.
Pediatric Nephrology (Berlin, Germany)
|
June 27, 2022
X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study
Louisa Bloudeau, Agnès Linglart, Sacha Flammier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 17, 2009
ACTH-independent Cushing's syndrome with bilateral micronodular adrenal hyperplasia and ectopic adrenocortical adenoma
Estelle Louiset, Françoise Gobet, Rossella Libé, et al.
Journal of Clinical Immunology
|
December 19, 2023
Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
Romain Lévy, Agathe Escudier, Paul Bastard, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 18, 2021
Prevalence of Enthesopathies in Adults With X-linked Hypophosphatemia: Analysis of Risk Factors
Julia Herrou, Axelle Salcion Picaud, Louis Lassalle, et al.
Orphanet Journal of Rare Diseases
|
October 26, 2023
XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)
Lothar Seefried, Ali Alzahrani, Pedro Arango Sancho, et al.
European Journal of Endocrinology
|
August 9, 2024
Metabolically healthy obesity in adults with X-linked hypophosphatemia
Anne-Lise Lecoq, Katharina Schilbach, Laurence Rocher, et al.
Molecular Genetics and Metabolism
|
February 7, 2021
Utility of genetic testing for prenatal presentations of hypophosphatasia
Brian Sperelakis-Beedham, Agnès Taillandier, Christelle Domingues, et al.
Clinical Endocrinology
|
February 17, 2012
Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours
Anya Rothenbuhler, Anelia Horvath, Rossella Libé, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
Plos One
|
October 27, 2017
Lower incidence of fracture after IV bisphosphonates in girls with Rett syndrome and severe bone fragility
Anne-Sophie Lambert, Anya Rothenbuhler, Perrine Charles, et al.
European Journal of Endocrinology
|
December 3, 2020
Inactivating PTH/PTHrP signaling disorders (iPPSDs): evaluation of the new classification in a multicenter large series of 544 molecularly characterized patients
Arrate Pereda, Francesca M Elli, Suzanne Thiele, et al.
Pediatric Nephrology (Berlin, Germany)
|
June 27, 2022
X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study
Louisa Bloudeau, Agnès Linglart, Sacha Flammier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 17, 2009
ACTH-independent Cushing's syndrome with bilateral micronodular adrenal hyperplasia and ectopic adrenocortical adenoma
Estelle Louiset, Françoise Gobet, Rossella Libé, et al.
Journal of Clinical Immunology
|
December 19, 2023
Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
Romain Lévy, Agathe Escudier, Paul Bastard, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 18, 2021
Prevalence of Enthesopathies in Adults With X-linked Hypophosphatemia: Analysis of Risk Factors
Julia Herrou, Axelle Salcion Picaud, Louis Lassalle, et al.
Orphanet Journal of Rare Diseases
|
October 26, 2023
XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)
Lothar Seefried, Ali Alzahrani, Pedro Arango Sancho, et al.
European Journal of Endocrinology
|
August 9, 2024
Metabolically healthy obesity in adults with X-linked hypophosphatemia
Anne-Lise Lecoq, Katharina Schilbach, Laurence Rocher, et al.
Molecular Genetics and Metabolism
|
February 7, 2021
Utility of genetic testing for prenatal presentations of hypophosphatasia
Brian Sperelakis-Beedham, Agnès Taillandier, Christelle Domingues, et al.
Clinical Endocrinology
|
February 17, 2012
Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours
Anya Rothenbuhler, Anelia Horvath, Rossella Libé, et al.
Page
of 8