X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia and is caused by mutation in the PHEX gene, resulting in excessive expression of the phosphaturic factor FGF23. Symptoms are mainly related to rickets in children and osteomalacia in adults and cause several complications that can be highly invalidating. Due to its rarity, XLH is poorly known and diagnosis is frequently delayed. Conventional treatment is based on oral phosphate salts supplementation and activated vitamin D analogs, which however, cannot cure the disease in most cases
X-linked hypophosphatemia (XLH) is a rare inheritable disorder of phosphate handling due to loss of ...
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is asso...
Purpose: X-linked hypophosphatemic rickets (XLH) is a rare genetic disease characterized by an incre...
Background: X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia...
Background X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia ...
BACKGROUND: X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function ...
X-linked hypophosphatemic rickets (XLH) is the commonest inherited form of rickets. It is caused by ...
X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in...
PDF formato impresiónX-Linked hypophosphatemia (XLH) is the most common form of hereditary rickets c...
Background X-linked hypophosphataemia (XLH) is a rare, hereditary, progressive and lifelong phosphat...
X-linked hypophosphatemic rickets (XLH) is an hereditary form of rickets due to isolated renal tubul...
X-linked hypophosphatemia (XLH) is the most common cause of rickets related to inherited renal phosp...
X-linked hypophosphatemia (XLH) is caused by mutations in the PHEX gene, which encodes a cell surfa...
X-linked hypophosphatemia (XLH) is a rare multisystemic disease with a prominent musculoskeletal phe...
Objective: To provide Italian expert opinion-based practical recommendations to improve the cooperat...
X-linked hypophosphatemia (XLH) is a rare inheritable disorder of phosphate handling due to loss of ...
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is asso...
Purpose: X-linked hypophosphatemic rickets (XLH) is a rare genetic disease characterized by an incre...
Background: X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia...
Background X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia ...
BACKGROUND: X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function ...
X-linked hypophosphatemic rickets (XLH) is the commonest inherited form of rickets. It is caused by ...
X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in...
PDF formato impresiónX-Linked hypophosphatemia (XLH) is the most common form of hereditary rickets c...
Background X-linked hypophosphataemia (XLH) is a rare, hereditary, progressive and lifelong phosphat...
X-linked hypophosphatemic rickets (XLH) is an hereditary form of rickets due to isolated renal tubul...
X-linked hypophosphatemia (XLH) is the most common cause of rickets related to inherited renal phosp...
X-linked hypophosphatemia (XLH) is caused by mutations in the PHEX gene, which encodes a cell surfa...
X-linked hypophosphatemia (XLH) is a rare multisystemic disease with a prominent musculoskeletal phe...
Objective: To provide Italian expert opinion-based practical recommendations to improve the cooperat...
X-linked hypophosphatemia (XLH) is a rare inheritable disorder of phosphate handling due to loss of ...
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is asso...
Purpose: X-linked hypophosphatemic rickets (XLH) is a rare genetic disease characterized by an incre...