Results 91 to 100 of about 445 (162)

Clinical and genetic characteristics of Chinese patients with congenital cranial dysinnervation disorders. [PDF]

open access: yesOrphanet J Rare Dis, 2022
Jia H   +12 more
europepmc   +1 more source

TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels. [PDF]

open access: yesJ Inherit Metab Dis, 2022
Muylle E   +11 more
europepmc   +1 more source

Wernicke's Encephalopathy Secondary to Cannabis Hyperemesis Syndrome. [PDF]

open access: yesJ Brown Hosp Med
Kattamuri L   +7 more
europepmc   +1 more source

Orbital Giant Cell Reparative Granuloma: A Case Report. [PDF]

open access: yesOphthalmic Plast Reconstr Surg
Wang N, Li J, Ma J.
europepmc   +1 more source

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