Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Aisha Al Qahtani"'
Autor:
Salma M. Wakil, Dorota Monies, Samya Hagos, Fahad Al-Ajlan, Josef Finsterer, Aisha Al Qahtani, Khushnooda Ramzan, Rawan Al Humaidy, Mohamed A. Al-Muhaizea, Brian Meyer, Saeed A. Bohlega
Publikováno v:
Case Reports in Genetics, Vol 2018 (2018)
Hereditary sensory and autonomic neuropathies (HSANs) are a clinically and genetically heterogeneous group of disorders involving various sensory and autonomic dysfunctions. The most common symptoms of HSANs include loss of sensations of pain and tem
Externí odkaz:
https://doaj.org/article/4e810ac4986442648d13395431f8d886
Autor:
Saeed Bohlega, Salma M. Wakil, Fahad S. Al-Ajlan, Mohamed A. Al-Muhaizea, Rawan Al Humaidy, Aisha Al Qahtani, Samya Hagos, Khushnooda Ramzan, Brian F. Meyer, Josef Finsterer, Dorota Monies
Publikováno v:
Case Reports in Genetics
Case Reports in Genetics, Vol 2018 (2018)
Case Reports in Genetics, Vol 2018 (2018)
Hereditary sensory and autonomic neuropathies (HSANs) are a clinically and genetically heterogeneous group of disorders involving various sensory and autonomic dysfunctions. The most common symptoms of HSANs include loss of sensations of pain and tem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3ced7e4e0a6d989b336f67db5e3b88
http://europepmc.org/articles/PMC6311306
http://europepmc.org/articles/PMC6311306
Publikováno v:
Healthcom
Ubiquitous availability of wireless and electronic devices has raised some health alarms among the masses. There exist possible malign effects of electromagnetic radiations on the human body, and especially on the brain due to existence of radio freq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ddfca116dfed9c62a7daac54bc4a523
https://doi.org/10.1109/healthcom.2013.6720780
https://doi.org/10.1109/healthcom.2013.6720780
Autor:
Wakil, Salma M.1, Monies, Dorota1, Hagos, Samya1, Al-Ajlan, Fahad2, Finsterer, Josef3, Al Qahtani, Aisha1, Ramzan, Khushnooda1, Al Humaidy, Rawan1, Al-Muhaizea, Mohamed A.2, Meyer, Brian1, Bohlega, Saeed A.2
Publikováno v:
Case Reports in Genetics. 12/12/2018, p1-5. 5p.