Manifestaciones neurológicas atípicas del síndrome de reconstitución inmunológico por infección con el virus de inmunodeficiencia humana, reporte de los casos

Bernal Cano, Francisco; Suárez, Jorge Oswaldo; Álvarez, Carlos Arturo; Lowenstein, Ellen; Valderrama, Sandra Liliana; Gómez, Carlos Hernando; Támara, José Roberto; Tenorio, Iván Ramiro.
Univ. med ; 52(1): 120-129, ene.-mar. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-620376

Documentos relacionados

  1. [Genetic analysis of a Chinese pedigree with Lesch-Nyhan syndrome].
  2. Congenital anomalies-associated Riga-Fede disease as an early manifestation of Lesch-Nyhan syndrome: rare entities in the same pediatric patient-a case report.
  3. [Analysis of HPRT1 gene variant and prenatal diagnosis for a Chinese pedigree with Lesch-Nyhan syndrome but no specimen from affected probands].
  4. Ethical implications of early genetic diagnosis in an infant with Lesch-Nyhan syndrome.
  5. PUS7 deficiency in human patients causes profound neurodevelopmental phenotype by dysregulating protein translation.
  6. Lesch-Nyhan syndrome due to a splice-site mutation in a 14-month-old boy presenting as acute renal failure.
  7. Abnormalities of neural stem cells in Lesch-Nyhan disease.
  8. Naringin corrects renal failure related to Lesch-Nyhan disease in a rat model via NOS-cAMP-PKA and BDNF/TrkB pathways.
  9. A new physiological medium uncovers biochemical and cellular alterations in Lesch-Nyhan disease fibroblasts.
  10. Deep brain stimulation in Lesch-Nyhan syndrome: a systematic review.