Results 101 to 110 of about 6,052 (162)

Endocrine disorders in a patient with a suspicion of a mitochondrial disease, MELAS syndrome - a case report and literature review. [PDF]

Pediatr Endocrinol Diabetes Metab, 2021
Baszyńska-Wilk M, Moszczyńska E, Szarras-Czapnik M, Wysocka-Mincewicz M, Wątrobińska U, Kozłowska A, Szalecki M.   +6 more
europepmc   +1 more source

Association between the habitual lip and tongue posture, clinical characteristics, and sleep-related problems in infants with Trisomy 21. [PDF]

Codas
Rezende GMG, Fernandes AER, Silva AVMV, Campos LM, Telson YC, Motta AR, Pretti H, Furlan RMMM.   +7 more
europepmc   +1 more source

[Angelman syndrome in adulthood]. [PDF]

Rev Neurol, 2023
Lorenzo-Ruiz M, Novo-Ponte S, Iglesias-Escalera G, Cazorla-Calleja R, Lara-Herguedas J, López-Pájaro LF, Ruiz-Antorán B.   +6 more
europepmc   +1 more source

[Spinal Muscular Atrophy: The Reality of the Adult Patient in Spain]. [PDF]

Rev Neurol
Cattinari MG, De Lemus M, Dumont M, Tizzano E.   +3 more
europepmc   +1 more source

Self-efficacy and breastfeeding outcomes in mothers of premature and term infants: a longitudinal study. [PDF]

Codas, 2023
Assunção DGF, Cruz MCLD, Holanda NSO, Fagundes RBB, Carvalho AVD, Azevedo IG, Pereira SA.   +6 more
europepmc   +1 more source

“ESTUDIO DEL NEURODESARROLLO EN INFANTES CON CARDIOPATÍAS CONGÉNITAS SEVERAS” [PDF]

, 2014
Esquivel Hernández, Francisco José, Otero Ojeda, Gloria Adelina   +1 more
core  

[Gross Motor Function after Rehabilitation with the Atlas 2030 Pediatric Exoskeleton in Children With Cerebral Palsy]. [PDF]

Rev Neurol
García Oliveros I, Meabe Iturbe N, Marín Ojea JI, Lancho Poblador C, Fuentes-Claramonte P, Quemada Ubis JI.   +5 more
europepmc   +1 more source

Paediatric motor phenotypes in early-onset ataxia, developmental coordination disorder, and central hypotonia. [PDF]

Dev Med Child Neurol, 2020
Lawerman TF, Brandsma R, Maurits NM, Martinez-Manzanera O, Verschuuren-Bemelmans CC, Lunsing RJ, Brouwer OF, Kremer HP, Sival DA.   +8 more
europepmc   +1 more source

[RYR1 myopathies in childhood: phenotype-genotype correlation and incidence]. [PDF]

Rev Neurol
Del Arco-Guzmán N, Lobato-López S, Calvo-Medina R, Vera-Medialdea R, Ruiz-Pérez C, Ramos-Fernández JM.   +5 more
europepmc   +1 more source

Figure-based speech perception test: applicability in children with Down syndrome. [PDF]

Codas, 2022
Gonçalves BN, Lorenssete IR, Tomé NO, Mota ALR, Garcia CFD, Reis ACMB.   +5 more
europepmc   +1 more source