Results 91 to 100 of about 8,926 (143)

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  

Síndromes do núcleo rubro. A propósito de três casos com etiologia sifilítica, um dos quais associado a mioclonias velofaringolaríngeas

Arquivos de Neuro-Psiquiatria, 1950
Registrando três casos de síndromes do núcleo rubro — dois de síndrome superior e um de síndrome inferior, tipo Claude — os autores revêem a anátomo-fisiologia dessa formação mesencefálica. Ressaltam particularmente as alterações do tono verificadas pela
Adherbal Tolosa, Horacio M. Canelas
doaj  

[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

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

[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

Factors associated with breastfeeding in infants with trisomy 21. [PDF]

Codas
Campos LM, Fernandes AER, Motta AR, Furlan RMMM.   +3 more
europepmc   +1 more source

[Copy number variation and parental consanguinity elevated in newborns of high altitude with major congenital anomalies in Perú]. [PDF]

Rev Fac Cien Med Univ Nac Cordoba, 2022
Abarca Barriga HH, Chavesta Velásquez F, Barletta Carrillo C, Paucarmayta Tacuri A, Bazán Hurtado M, Vásquez Loarte T, Ordoñez Rondón L, Ordoñez Linares M, Rondón Abuhadba EA.   +8 more
europepmc   +1 more source