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متلازمة غوميز-لوبيز-هيرنانديز (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة غوميز-لوبيز-هيرنانديز" in Arabic language version.

refsWebsite
Global rank Arabic rank
10nih.gov
4th place
6th place
9doi.org
2nd place
5th place
4semanticscholar.org
11th place
86th place
1web.archive.org
1st place
1st place
1uzh.ch
3,633rd place
4,746th place
1worldcat.org
5th place
4th place

doi.org

  • Fernández-Jaén A، Fernández-Mayoralas DM، Calleja-Pérez B، Muñoz-Jareño N، Moreno N (2009). "Gomez-Lopez-Hernandez syndrome: two new cases and review of the literature". Pediatr Neurol. ج. 40 ع. 1: 58–62. DOI:10.1016/j.pediatrneurol.2008.10.001. PMID:19068257.
  • de Mattos VF، Graziadio C، Machado Rosa RF، Lenhardt R، Alves RP، Trevisan P، Paskulin GA، Zen PR (2014). "Gómez-López-Hernández syndrome in a child born to consanguineous parents: new evidence for an autosomal-recessive pattern of inheritance?". Pediatr Neurol. ج. 50 ع. 6: 612–5. DOI:10.1016/j.pediatrneurol.2014.01.035. PMID:24690526.
  • Gómez MR (1979). "Cerebellotrigeminal and focal dermal dysplasia: a newly recognized neurocutaneous syndrome". Brain Dev. ج. 1 ع. 4: 253–6. DOI:10.1016/s0387-7604(79)80039-x. PMID:95427. S2CID:4698879.
  • Gomy I، Heck B، Santos AC، Figueiredo MS، Martinelli CE Jr، Nogueira MP، Pina-Neto JM (2008). "Two new Brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights". Am J Med Genet A. ج. 146A ع. 5: 649–57. DOI:10.1002/ajmg.a.32173. PMID:18247421. S2CID:6105360.
  • Sukhudyan B، Jaladyan V، Melikyan G، Schlump JU، Boltshauser E، Poretti A (2013). "Gómez-López-Hernández syndrome: reappraisal of the diagnostic criteria" (PDF). Eur. J. Pediatr. ج. 169 ع. 12: 1523–8. DOI:10.1007/s00431-010-1259-7. PMID:20652311. S2CID:7101190. مؤرشف من الأصل (PDF) في 2023-05-11.
  • Poretti A، Bartholdi D، Gobara S، Alber FD، Boltshauser E (2008). "Gomez-Lopez-Hernandez syndrome: an easily missed diagnosis". Eur J Med Genet. ج. 51 ع. 3: 198–208. DOI:10.1016/j.ejmg.2008.01.004. PMID:18342593.
  • Kobayashi Y، Kawashima H، Magara S، Akasaka N، Tohyama J (2015). "Gómez-López-Hernández syndrome in a Japanese patient: a case report". Brain Dev. ج. 37 ع. 3: 356–8. DOI:10.1016/j.braindev.2014.05.002. PMID:24856766. S2CID:28604985.
  • Choudhary، Neha؛ Prabhakar، Anuj؛ Bhatia، Vikas؛ Gupta، Parul Chawla (19 أكتوبر 2021). "Gomez-López-Hernandez syndrome: the triad of cerebello-trigemino-dermal dysplasia". BMJ Case Reports. ج. 14 ع. 10: e246189. DOI:10.1136/bcr-2021-246189. ISSN:1757-790X. PMC:8527131. PMID:34667053.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: PMC embargo expired (link)
  • López-Hernández, A (2013). "Craniosynostosis, ataxia, trigeminal anaesthesia and parietal alopecia with pons-vermis fusion anomaly (atresia of the fourth ventricle). Report of two cases". Neuropediatrics. ج. 13 ع. 2: 99–102. DOI:10.1055/s-2008-1059606. PMID:7133329.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Fernández-Jaén A، Fernández-Mayoralas DM، Calleja-Pérez B، Muñoz-Jareño N، Moreno N (2009). "Gomez-Lopez-Hernandez syndrome: two new cases and review of the literature". Pediatr Neurol. ج. 40 ع. 1: 58–62. DOI:10.1016/j.pediatrneurol.2008.10.001. PMID:19068257.
  • de Mattos VF، Graziadio C، Machado Rosa RF، Lenhardt R، Alves RP، Trevisan P، Paskulin GA، Zen PR (2014). "Gómez-López-Hernández syndrome in a child born to consanguineous parents: new evidence for an autosomal-recessive pattern of inheritance?". Pediatr Neurol. ج. 50 ع. 6: 612–5. DOI:10.1016/j.pediatrneurol.2014.01.035. PMID:24690526.
  • Gómez MR (1979). "Cerebellotrigeminal and focal dermal dysplasia: a newly recognized neurocutaneous syndrome". Brain Dev. ج. 1 ع. 4: 253–6. DOI:10.1016/s0387-7604(79)80039-x. PMID:95427. S2CID:4698879.
  • Gomy I، Heck B، Santos AC، Figueiredo MS، Martinelli CE Jr، Nogueira MP، Pina-Neto JM (2008). "Two new Brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights". Am J Med Genet A. ج. 146A ع. 5: 649–57. DOI:10.1002/ajmg.a.32173. PMID:18247421. S2CID:6105360.
  • Sukhudyan B، Jaladyan V، Melikyan G، Schlump JU، Boltshauser E، Poretti A (2013). "Gómez-López-Hernández syndrome: reappraisal of the diagnostic criteria" (PDF). Eur. J. Pediatr. ج. 169 ع. 12: 1523–8. DOI:10.1007/s00431-010-1259-7. PMID:20652311. S2CID:7101190. مؤرشف من الأصل (PDF) في 2023-05-11.
  • Poretti A، Bartholdi D، Gobara S، Alber FD، Boltshauser E (2008). "Gomez-Lopez-Hernandez syndrome: an easily missed diagnosis". Eur J Med Genet. ج. 51 ع. 3: 198–208. DOI:10.1016/j.ejmg.2008.01.004. PMID:18342593.
  • Kobayashi Y، Kawashima H، Magara S، Akasaka N، Tohyama J (2015). "Gómez-López-Hernández syndrome in a Japanese patient: a case report". Brain Dev. ج. 37 ع. 3: 356–8. DOI:10.1016/j.braindev.2014.05.002. PMID:24856766. S2CID:28604985.
  • Choudhary، Neha؛ Prabhakar، Anuj؛ Bhatia، Vikas؛ Gupta، Parul Chawla (19 أكتوبر 2021). "Gomez-López-Hernandez syndrome: the triad of cerebello-trigemino-dermal dysplasia". BMJ Case Reports. ج. 14 ع. 10: e246189. DOI:10.1136/bcr-2021-246189. ISSN:1757-790X. PMC:8527131. PMID:34667053.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: PMC embargo expired (link)
  • López-Hernández, A (2013). "Craniosynostosis, ataxia, trigeminal anaesthesia and parietal alopecia with pons-vermis fusion anomaly (atresia of the fourth ventricle). Report of two cases". Neuropediatrics. ج. 13 ع. 2: 99–102. DOI:10.1055/s-2008-1059606. PMID:7133329.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

uzh.ch

zora.uzh.ch

web.archive.org

worldcat.org