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Emese Boros, Iva Gueorguieva, Anya Rothenbuhler, Agnès Linglart, Justine Bacchetta, Régis Coutant, Thomas Edouard, Jean Pierre Salles, Valerie Porquet Bordes, Barbara Girerd, Brigitte Mignot, Volha Zhukouskaya, Cyril Amouroux, Karine Briot, Peter Kamenicky, Anne Lise Lecoq, Christelle Audrain, Jugurtha Berkenou, Diana-Alexandra Ertl

European journal of endocrinology 2023;189(4):469-475

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Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia.

Wolfgang Högler, Lothar Seefried, Maria Luisa Brandi, Kassim M Javaid, Deborah Eastwood, Gema Ariceta, Agnès Linglart, Lars Rejnmark, Peter Kamenický, Elena Levtchenko, Dieter Haffner, Catherine Chaussain, Justine Bacchetta, Federico Di Rocco, Detlef Bockenhauer, Francesco Emma, Karine Briot, Dirk Schnabel, Philippe Wicart, Lars Savendahl, Martha Kirchhoff, Pol Harvengt, Martin Biosse Duplan, Oliver Gardiner

Nature reviews. Nephrology 2025;21(5):330-354

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Congenital Conditions of Hypophosphatemia Expressed in Adults.

Maria Luisa Brandi, Gemma Marcucci

Calcified tissue international 2021;108(1):91-103

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X-linked hypophosphataemia.

Agnès Linglart, Peter Kamenický, Craig F Munns, Karine Briot

Lancet (London, England) 2024;404(10455):887-901

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Characterization of Oral Health Status in Chilean Patients with X-Linked Hypophosphatemia.

Pablo Florenzano, Michael T Collins, Danisa Ivanovic-Zuvic, Eugenia Borja, Macarena Jiménez, Pilar Morales, Alejandro Marin

Calcified tissue international 2021;109(2):132-138

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Insight into Natural History and Phenotype in Untreated Adults with X-Linked Hypophosphatemia.

Giampiero I Baroncelli, Filomena Cetani, Benedetta Toschi, Alessandra Bulleri, Alessandro Isola, Maria Rita Giuca, Elisabetta Carli, Maria Rita Sessa, Caterina Pelosini, Angela Michelucci, Pasquale Comberiati

Calcified tissue international 2026;117(1):

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Genetic causes of hypophosphatemia.

Nuria Puente, Jose A Riancho, Pablo Solis

Minerva medica 2024;115(3):320-336

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Contemporary Medical and Surgical Management of X-linked Hypophosphatemic Rickets.

Melinda S Sharkey, Karl Grunseich, Thomas O Carpenter

The Journal of the American Academy of Orthopaedic Surgeons 2015;23(7):433-42

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Results for ""PHEX Phosphate Regulating Neutral Endopeptidase""[mesh_terms]

PHEX gene and hypophosphatemia.

Molecular pathogenesis of hypophosphatemic rickets.

Genetic advances, biochemical and clinical features and critical approach to treatment of patients with X-linked hypophosphatemic rickets.

Case Report: A case of x-linked hypophosphatemic rickets complicated with polyostotic fibrous dysplasia caused by PHEX gene mutation and literature review.

PHEX gene mutation in a Chinese family with six cases of X-linked hypophosphatemic rickets.

X-linked hypophosphatemic rickets: Description of seven new variants in patients followed up in reference hospitals in Rio de Janeiro.

Tumor-induced osteomalacia and the regulation of phosphate homeostasis.

Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study.

Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia.

Congenital Conditions of Hypophosphatemia Expressed in Adults.

X-linked hypophosphataemia.

Characterization of Oral Health Status in Chilean Patients with X-Linked Hypophosphatemia.

Insight into Natural History and Phenotype in Untreated Adults with X-Linked Hypophosphatemia.

Genetic causes of hypophosphatemia.

Contemporary Medical and Surgical Management of X-linked Hypophosphatemic Rickets.

Results for

""PHEX Phosphate Regulating Neutral Endopeptidase""[mesh_terms]