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Síndrome de Gilbert (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome de Gilbert" in Spanish language version.

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11nih.gov
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1nhs.uk
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doi.org

dx.doi.org

  • Kohle C, Mohrle B, Munzel PA, Schwab M, Wernet D, Badary OA, Bock KW (2003). «Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians.». Biochem Pharmacol 65 (9): 1521-7. PMID 12732365. doi:10.1016/S0006-2952(03)00074-1. 
  • Larissa K. F. Temple, Robin S. McLeod, Steven Gallinger, James G. Wright (2001). «Defining Disease in the Genomics Era». Science Magazine 293 (5531): 807-808. doi:10.1126/science.1062938. 

emedicine.com

gilbertssyndrome.com

harrisonmedicina.com

iqb.es

liverfoundation.org

news-medical.net

nhs.uk

nih.gov

ncbi.nlm.nih.gov

  • Marcuello E, Altés A, Menoyo A, Del Rio E, Gómez-Pardo M, Baiget M (2004). «UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer.». Br J Cancer 91 (4): 678-82. PMID 15280927. 
  • Rauchschwalbe S, Zuhlsdorf M, Wensing G, Kuhlmann J (2004). «Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype.». Int J Clin Pharmacol Ther 42 (2): 73-7. PMID 15180166. 
  • Kohle C, Mohrle B, Munzel PA, Schwab M, Wernet D, Badary OA, Bock KW (2003). «Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians.». Biochem Pharmacol 65 (9): 1521-7. PMID 12732365. doi:10.1016/S0006-2952(03)00074-1. 
  • Esteban A, Pérez-Mateo M (1999). «Heterogeneity of paracetamol metabolism in Gilbert's syndrome». European journal of drug metabolism and pharmacokinetics 24 (1): 9-13. PMID 10412886. 
  • Gitlin N. (1977). «The clinical presentation of Gilbert's disease in 26 patients.». South Africa Medical Journal 52 (1): 19-20. PMID 888039. 
  • Olsson R, Bliding A, Jagenburg R, Lapidus L, Larsson B, Svärdsudd K, Wittboldt S. (1988). «Gilbert's syndrome--does it exist? A study of the prevalence of symptoms in Gilbert's syndrome.». Acta Med Scandinavia 224 (5): 485-490. PMID 3264448. 
  • Gilbert syndrome, UGT1A1*28 allele, and cardiovascular disease risk: possible protective effects and therapeutic applications of bilirubin. Pubmed.

nlm.nih.gov

ghr.nlm.nih.gov

omim.org

orpha.net

rarediseases.org

  • «Gilbert Syndrome». NORD (National Organization for Rare Disorders) (en inglés estadounidense). Consultado el 16 de noviembre de 2022. 

sagepub.com

journals.sagepub.com

scielo.cl

spars.es

  • Urgel Gómez, M.T.; Fleta Zaragozano, J.; Lázaro Almarza, A.; López Moreno, M.J.; Olivares López, J.L. (enero de 2005). «Síndrome de Gilbert». Bol Pediatr Arag Rioj Sor 35 (1-2): 14-16. Consultado el 13 de junio de 2017. 

ufm.edu

medicina.ufm.edu

  • "El síndrome de Gilbert [...] por lo general no presenta síntomas, aunque una leve ictericia puede aparecer en condiciones de esfuerzo excesivo, estrés, insomnio, cirugías, ayuno, cuando hay infecciones o tras la ingesta de algunos medicamentos como el paracetamol, ya que la concentración de bilirrubina en la sangre aumenta en estas situaciones. El síndrome causa fatiga y depresión.". Facultad de Medicina de la Universidad Francisco Marroquín Archivado el 8 de febrero de 2017 en Wayback Machine.

web.archive.org