Ausgabe Sonderheft 2/2020
Supplement Issue: X‐Linked Hypophosphatemic Rickets
Inhalt (13 Artikel)
Genetic Diagnosis of Rare Diseases: Past and Present
Feliciano Ramos-Fuentes, Antonio González-Meneses, Elisabet Ars, Julio Hernández-Jaras
Albuminuria Downregulation of the Anti-Aging Factor Klotho: The Missing Link Potentially Explaining the Association of Pathological Albuminuria with Premature Death
Beatriz Fernández-Fernández, Lara Valiño-Rivas, Maria D. Sánchez-Niño, Alberto Ortiz
Hypophosphataemic Rickets: Similar Phenotype of Different Diseases
Francisco de la Cerda-Ojeda, Juan D. González-Rodríguez, Leire Madariaga, Guillermo Martínez-Díaz-Guerra, María L. Matoses-Ruipérez
Usefulness of X-rays in the Differential Diagnosis of Hypophosphataemic Rickets
José Martel-Villagrán, Ana Arias-Medina, Gloria García-Mardones
Hypophosphataemic Rickets: Diagnosis Algorithm—How Not to Make a Mistake
Domingo González-Lamuño
Complications of Phosphate and Vitamin D Treatment in X-Linked Hypophosphataemia
Pedro Arango Sancho
Panel Discussion: Some Aspects of the Management of Patients with X-Linked Hypophosphataemic Rickets
José-Vicente Torregrosa, Jaime Sánchez del Pozo, María Isabel Luiz Yanes, Manuel Muñoz Torres