Results 151 to 160 of about 26,453 (213)

Advancing patient evidence in XLH (APEX): rationale and design of a real-world XLH global data unification program. [PDF]

open access: yesFront Endocrinol (Lausanne)
Brandi ML   +7 more
europepmc   +1 more source

Raine Syndrome (OMIM #259775), Caused By FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660)

open access: yesJournal of Bone and Mineral Research, 2017
M. Whyte   +8 more
semanticscholar   +1 more source

Tumour in the dark: a challenging case of osteomalacia. [PDF]

open access: yesOxf Med Case Reports
Ambrogetti R   +4 more
europepmc   +1 more source

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