Results 91 to 100 of about 1,671 (180)

Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry. [PDF]

open access: yesOrphanet J Rare Dis
Sanson B   +33 more
europepmc   +1 more source

Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort study. [PDF]

open access: yesEur J Neurol
Barbat du Closel L   +21 more
europepmc   +1 more source

Medical management pathways for Cushing's disease in pituitary tumors centers of excellence (PTCOEs). [PDF]

open access: yesPituitary
Giustina A   +18 more
europepmc   +1 more source

Correction to: Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP‑mediated disease reveals characteristic features useful for diagnosis. [PDF]

open access: yesJ Neurol
Esteller D   +65 more
europepmc   +1 more source

Newborn Screening for Metachromatic Leukodystrophy: A Systematic Literature Review. [PDF]

open access: yesInt J Neonatal Screen
Laugwitz L   +5 more
europepmc   +1 more source

Standards of care for medical management of acromegaly in pituitary tumor centers of excellence (PTCOE). [PDF]

open access: yesPituitary
Giustina A   +18 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy