Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gururaj Aithala Kodavooru"'
Publikováno v:
Dubai Medical Journal, Pp 133-135 (2022)
COVID-19, caused by novel coronavirus SARS-CoV-2, which seemed to have unaffected the children in the initial period of the pandemic, now has targeted the pediatric population with varied clinical manifestations; the pathophysiology is still under ex
Externí odkaz:
https://doaj.org/article/80936712d7c64fc993f424b4c7b08918
Autor:
Muzammil Hafeez, Mahmoud Ahmed Galal, Anwar Khan, Gururaj Aithala Kodavooru, Hussein Z Adamjee Burhani, Yaser Husain Morsy El Saba, Rashid Mustafa, Manal Zaki Younis
Publikováno v:
Hamdan Medical Journal, Vol 13, Iss 4, Pp 235-238 (2020)
Joubert syndrome (OMIM 213300) is an uncommon autosomal recessive disorder that is characterised by distinct mid-hindbrain abnormalities, hypotonia and developmental delay. The molar tooth sign is a distinctive radiological feature of Joubert Syndrom
Autor:
Cristina Skrypnyk, Abubaker Al Madani, Mohammed Jan, André Mégarbané, Khalid Al Thihli, Ali Al Shehri, Abdulaziz Al Saman, Mohammad Al Muhaizea, Waseem Fathalla, Andoni Urtizberea, Gholamreza Zamani, Sylvie Tuffery-Giraud, Carlos Ignacio Ortez González, Pawan Kashyape, Ahmed Al Rumayyan, Edward Cupler, Laila Bastaki, Mohammed Al Jumah, Gururaj Aithala Kodavooru
Publikováno v:
Neurodegenerative Disease Management
Aim: Duchenne muscular dystrophy (DMD) is a severe and rare X-linked neuromuscular childhood disorder that results in functional decline, loss of ambulation and early death due to cardiac or respiratory failure. The objective of this paper is to addr