Erdheim-Chester disease and slowly progressive cerebellar dysfunction

Por BOHLEGA, S., FUKAZAWA, T.
Publicado em 1998

Novel mutation of the notch3 gene in arabic family with CADASIL

Por Bohlega, Saeed
Publicado em 2011

The Burden of Musculoskeletal Conditions at the Start of the New Millennium

Por Bohlega, Saeed
Publicado no Ann Saudi Med (2004)

Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation

Por Alqwaifly, Mohammed, Bohlega, Saeed
Publicado no Neurol Int (2016)

Riboflavin Has Neuroprotective Potential: Focus on Parkinson’s Disease and Migraine

Por Marashly, Eyad T., Bohlega, Saeed A.
Publicado no Front Neurol (2017)

Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalation

Por SAEED BOHLEGA, Walaa B Mohammed, Salma Tarabzouni
Publicado em 2022-05-01

Absence of mtDNA mutations in leukocytes of CADASIL patients

Por Abu-Amero, Khaled K, Hellani, Ali, Bohlega, Saeed
Publicado em 2008

Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues

Por Bohlega, Saeed, Al-Ajlan, Huda, Al-Saif, Amr
Publicado em 2014

Localization of the Gene for a Novel Autosomal Recessive Neurodegenerative Huntington-Like Disorder to 4p15.3

Por Kambouris, M., Bohlega, S., Al-Tahan, A., Meyer , B. F.
Publicado em 2000

Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation

Por Abu-Amero, K K, Bosley, T M, Bohlega, S, McLean, D
Publicado em 2005

Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegia.

Por Khan, S, Yaqub, B A, Poser, C M, al Deeb, S M, Bohlega, S
Publicado em 1995

Oromandibular Dystonia in Yemeni Patients with Khat Chewing: A Response to Botulinum Toxin Treatment

Por Shehata, Hatem S., El-Tamawy, Mohamed S., Mohieldin, Nevin, Edrees, Mohammed, Bohlega, Saeed
Publicado em 2014

Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer’s dyskinesia

Por Alshubaili, Asmahan, Abou-Al-Shaar, Hussam, Santhamoorthy, Ponnusamy, Attia, Hosam, Bohlega, Saeed
Publicado no BMC Neurol (2016)

A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Por Abu-Amero, Khaled K, Al-Dhalaan, Hesham, Bohlega, Saeed, Hellani, Ali, Taylor, Robert W
Publicado em 2009

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation

Por Hdiji, Olfa, Turki, Emna, Bouzidi, Nouha, Bouchhima, Imen, Damak, Mariem, Bohlega, Saeed, Mhiri, Chokri
Publicado no J Mov Disord (2016)

Huntington's disease in Saudi Arabia.

Por Bohlega, S, McLean, D, Omer, S, al Kawi, Z, Roos, R A, Losekoot, M, Bakker, E
Publicado em 1995

Multiple sclerosis in the Arabian Gulf countries: a consensus statement

Por Bohlega, Saeed, Inshasi, Jihad, Al Tahan, Abdel Rahman, Madani, Abu Bakr, Qahtani, Hussien, Rieckmann, Peter
Publicado em 2013

Hypotonic fluids after liver transplantation may be associated with prolonged ICU stay

Por Nadeem, A, Salahuddin, N, ElHazmi, A, Joseph, M, Bohlega, B, Sallam, H, Elsheikh, Y, Broering, D
Publicado em 2014

Chloride-liberal fluids are associated with acute kidney injury after liver transplantation

Por Nadeem, Ashraf, Salahuddin, Nawal, El Hazmi, Alyaa, Joseph, Mini, Bohlega, Balsam, Sallam, Hend, Sheikh, Yasser, Broering, Dieter
Publicado no Crit Care (2014)

Clinical and genetic features of anoctaminopathy in Saudi Arabia

Por Bohlega, Saeed, Monies, Dorothy M., Abulaban, Ahmad A., Murad, Hatem N., Alhindi, Hindi N., Meyer, Brian F.
Publicado no Neurosciences (Riyadh) (2015)