Results 91 to 100 of about 9,026 (144)

Patología podológica en el paciente con Síndrome de Down. Revisión bibliográfica

, 2017
Treball Final de Grau de Podologia, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, curs: 2016-2017, Tutor: Baldiri Prats ClimentEl Síndrome de Down es la alteración cromosómica más habitual en la población.
López Andrés, Cristina
core  

A criança com necessidades especiais no projeto de Equoterapia da UNESP

Revista Ciência em Extensão, 2011
O Projeto de Extensão Universitária "EQUOTERAPIA: uma atividade motora para o desenvolvimento de Pessoas com deficiências" tem como objetivo oferecer atividades motoras para pessoas com deficiências, promovendo o desenvolvimento dos aspectos ...
Fernanda Carolina Toledo Silva, Marli Nabeiro, Vanessa Fernandes, Roberta Daroz, Aveline Rocha Lima da Silva, Débora Gambary Freire   +5 more
doaj  

[Temporomandibular manifestation in patients with Ehlers-Danlos syndrome: a systematic review]. [PDF]

Rev Cient Odontol (Lima), 2023
Cancino J, Soto F, Martinez S, Gutiérrez S.   +3 more
europepmc   +1 more source

The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype. [PDF]

Pediatr Endocrinol Diabetes Metab, 2022
Wesół-Kucharska D, Rokicki D, Greczan M, Kaczor M, Czekuć-Kryśkiewicz E, Piekutowska-Abramczuk D, Halat-Wolska P, Ciara E, Jaworski M, Jezela-Stanek A.   +9 more
europepmc   +1 more source

Surgical complications in 2,840 cases of hemorrhoidectomy by Milligan-Morgan, Ferguson and combined techniques

Journal of Coloproctology, 2012
The analysis of 2,840 cases of hemorrhoidectomy by open techniques of Milligan-Morgan (2,189 cases), Ferguson (341 cases) and mixed (310 cases) in 11,043 patients with hemorrhoidal disease (HD) allowed the following conclusions.
Guilherme de Almeida Santos, Caroline Pinto Coutinho, Matheus Matta Machado Mafra Duque Estrada Meyer, Diego Vieira Sampaio, Geraldo Magela Gomes da Cruz   +4 more
doaj  

Clinical-functional characterization of patients with spinal muscular atrophy in Central-Western Colombia [PDF]

Biomedica, 2022
Cardona N, Ocampo SJ, Estrada JM, Mojica MI, Porras GL.   +4 more
europepmc   +1 more source

[Neurodevelopmental and Movement Disorder Due to a Mutation in the GNAO1 Gene: A Case Report]. [PDF]

Rev Neurol
Hernández Yeneris SM, González-Solano MA, Lince-Rivera I, Rojas-Martínez JA, Ramón-Gómez JL.   +4 more
europepmc   +1 more source

[Applicability of the London Classification to Characterize Defecation Disorders: a Retrospective Study in a Tertiary Care Center in Argentina]. [PDF]

Acta Gastroenterol Latinoam
Santana M, Piskorz MM, Tevez A, Gutierrez Arispe F, Acquafresca C, Uehara T, González Ballerga E, Olmos JA.   +7 more
europepmc   +1 more source

Orofacial myofunctional therapy associated with the use of the stimulating palatal plate in children with trisomy 21: case studies. [PDF]

Codas, 2023
Ferreira JEA, Almeida BRS, Deps TD, Pretti H, Furlan RMMM.   +4 more
europepmc   +1 more source

First report of PURA syndrome in a Colombian patient with de novo missense variant c.692T>C (p.Phe231Ser) [PDF]

Biomedica
Cerón SM, Pérez DA, Montaño JH, Acosta MA.   +3 more
europepmc   +1 more source