Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Gururaj, Aithala"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::77736f4b9a6bd98e8c01a2122707bb16
http://www.hamdanjournal.org/article.asp?issn=2227-2437
http://www.hamdanjournal.org/article.asp?issn=2227-2437
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2083e73b42e1499b6778e9dd983e38a
https://doi.org/10.2217/nmt-2019-0002
https://doi.org/10.2217/nmt-2019-0002
Publikováno v:
In Journal of Psychosomatic Research 2006 61(3):343-347
Autor:
Eapen, Valsamma, Zoubeidi, Taoufik, Yunis, Feisal, Gururaj, Aithala K., Sabri, Sufyan, Ghubash, Rafia
Publikováno v:
In Journal of Psychosomatic Research 2006 61(3):321-326
Autor:
Samar Almuntaser, Gururaj Aithala
Publikováno v:
Abstracts.
Colloid cysts are congenital benign lesions constituting 1% of CNS tumors. Pediatric colloid cysts are rare lesions compared with adults. These are more common in the third and fifth decade. Their occurrence in the pediatric age group is less commonl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec3b9b1f6a9c20f35dee27492dc93052
https://doi.org/10.1136/archdischild-2019-epa.984
https://doi.org/10.1136/archdischild-2019-epa.984
Autor:
Dixon-Salazar, Tracy, Silhavy, Jennifer L., Marsh, Sarah E., Louie, Carrie M., Scott, Lesley C., Gururaj, Aithala, Al-Gazali, Lihadh, Al-Tawari, Asma A., Kayserili, Hulya, Sztriha, László, Gleeson, Joseph G.
Publikováno v:
In The American Journal of Human Genetics 2004 75(6):979-987
Publikováno v:
Dubai Medical Journal; 2022, Vol. 5 Issue 3, p203-205, 3p
Autor:
Abdul Rezzak Hamzeh, Pratibha Nair, Fatma Bastaki, Majdi El-Halik, Madiha Mohamed, Fatima Saif, Mahmoud Taleb Al-Ali, Nafisa Tawfiq, Gururaj Aithala
Publikováno v:
Congenital Anomalies. 56:135-137
The WDR62 gene encodes a scaffold protein of the c-Jun N-terminal kinase (JNK) pathway. It plays a critical role in laying out various cellular layers in the cerebral cortex during embryogenesis, and hence the dramatic clinical features resulting fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83431c4d7dbb7f94bb7bfa1ad0e27483
https://doi.org/10.1111/cga.12144
https://doi.org/10.1111/cga.12144
Autor:
Fatma, Bastaki, Madiha, Mohamed, Pratibha, Nair, Fatima, Saif, Nafisa, Tawfiq, Gururaj, Aithala, Majdi, El-Halik, Mahmoud, Al-Ali, Abdul Rezzak, Hamzeh
Publikováno v:
Congenital anomalies. 56(3)
The WDR62 gene encodes a scaffold protein of the c-Jun N-terminal kinase (JNK) pathway. It plays a critical role in laying out various cellular layers in the cerebral cortex during embryogenesis, and hence the dramatic clinical features resulting fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c704c97a42be3d38904fb44fa61127f
https://pubmed.ncbi.nlm.nih.gov/26577670
https://pubmed.ncbi.nlm.nih.gov/26577670