Results 121 to 130 of about 7,684 (185)

[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

[Comportamiento y decisión cardiovascular en el síndrome de MASS. Reporte de un caso y revisión de la literatura]. [PDF]

Arch Cardiol Mex, 2021
Gómez-González MD, Tapia-Paredes M, Colín-Lizalde LJ, González-Ruíz F, Herrera-Alarcón V, Soto-López ME.   +5 more
europepmc   +1 more source

Bases anat?micas de las escoliosis

, 1998
Trabajo de Grado realizado en el Departamento de Anatom?a e Histolog?a Humanas de la Universidad de Salamanca.
openaire   +1 more source

Fragile X Syndrome in children. [PDF]

Colomb Med (Cali), 2023
Acero-Garcés DO, Saldarriaga W, Cabal-Herrera AM, Rojas CA, Hagerman RJ.   +4 more
europepmc   +1 more source

Evaluation of the Toxicity of Bisphenol A in Reproduction and Its Effect on Fertility and Embryonic Development in the Zebrafish (Danio rerio). [PDF]

Int J Environ Res Public Health, 2022
Reis LPG, Lora-Benítez AJ, Molina-López AM, Mora-Medina R, Ayala-Soldado N, Moyano-Salvago MDR.   +5 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

[Juvenile Pompe disease: Undescribed genotype. First report in Quintana Roo]. [PDF]

Rev Med Inst Mex Seguro Soc
Flores-Gonzale A, Herrera-Del Valle LE, Lara-Ramírez VR, Marco-Valdez I, Torres-Pedroza AJ, Briceño-Rodas KJ.   +5 more
europepmc   +1 more source

[Autosomal recessive limb-girdle muscular dystrophy-10. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Arzola AA, Juárez-Melchor D, Crisanto-López IE, Vera-Loaiza A, Hernández-Castañeda Y, Guzmán-Santiago TA, Jiménez-Pérez B, Rodríguez-Hurtado PO, Salazar-Bonilla W.   +8 more
europepmc   +1 more source

[X-linked intellectual disability syndrome with macrocephaly due to BRWD3 gene deletion]. [PDF]

Rev Neurol
Arroyo-Carrera I, Romero-Peguero R, Martín-Fernández R, Ramajo-Polo A, García-Navas Núñez V.   +4 more
europepmc   +1 more source

[Natural history of mucopolysaccharidosis type III in a series of Colombian patients]. [PDF]

Rev Neurol
Cabarcas L, Ramón JL, Espinosa E, Guerrero GP, Martínez N, Santamaría N, Lince I, Reyes S.   +7 more
europepmc   +1 more source