Results 111 to 120 of about 32,974 (204)

Pain in Children and Adolescents with Spinal Muscular Atrophy: A Longitudinal Study from a Patient Registry. [PDF]

open access: yesChildren (Basel), 2023
Pitarch-Castellano I   +8 more
europepmc   +1 more source

Atrofia muscular espinal tipo II: un caso atípico.

open access: yes, 2019
Spinal Muscular Atrophy (SMA) is a recessive genetic disease that produces a degeneration and loss of the motor neurons, which turn into a denervation and muscle weakness. This happens because of a mutation or a deletion of the SMN1 and SMN2 genes, which result in the exon 7 of the RNA.
Díaz Álvarez, Efrén   +1 more
openaire   +1 more source

Type-1 spinal muscular atrophy cohort before and after disease-modifying therapies. [PDF]

open access: yesArq Neuropsiquiatr
Alves BKAMF   +3 more
europepmc   +1 more source

Why should a 5q spinal muscular atrophy neonatal screening program be started? [PDF]

open access: yesArq Neuropsiquiatr
Becker MM   +5 more
europepmc   +1 more source

Cerebral and cerebellar pseudoatrophy associated with valproic acid. Report of three pediatric cases. [PDF]

open access: yesRev Neurol, 2023
Ordoño-Saiz MV   +10 more
europepmc   +1 more source

X-linked spinal and bulbar muscular atrophy (Kennedy's disease): the first case described in the Brazilian Amazon. [PDF]

open access: yesEinstein (Sao Paulo), 2018
Alves CN   +5 more
europepmc   +1 more source

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