Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Rami Alhazmi"'
Autor:
Ali Mir, Tarek Jallul, Faisal Alotaibi, Fawzia Amer, Ahmed Najjar, Rami Alhazmi, Mona Al Faraidy, Alanoud Alharbi, Fatimah Aldurayhim, Zakia Barnawi, Bassam Fallatah, Mona Ali, Husam Almuhaish, Fadhel Almolani, Abdullah Suwailem, Mahmoud Tuli, Abdulrahman Naim, Suad Hassan, Brent Hedgcock, Ghadah Bostanji, Shahid Bashir, Raidah AlBaradie
Publikováno v:
Epilepsia Open, Vol 8, Iss 3, Pp 930-945 (2023)
Abstract Objective Epilepsy surgery is widely accepted as an effective therapeutic option for carefully selected patients with drug‐resistant epilepsy (DRE). There is limited data on the outcome of epilepsy surgery, especially in pediatric patients
Externí odkaz:
https://doaj.org/article/53bf66947ef44133897432c37c4d1ae0
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 429-433 (2021)
MEGDEL 3-methylglutaconic (MG) aciduria, deafness, encephalopathy, Leigh-like syndrome is an autosomal recessive disorder associated with infantile hypoglycemia, progressive psychomotor developmental delay, cerebellar atrophy with lesions in the basa
Externí odkaz:
https://doaj.org/article/92e140e7c71140a7992099dd9cdd64eb
Publikováno v:
Radiology Case Reports, Vol 15, Iss 11, Pp 2339-2342 (2020)
Our case involved a 1-year-old female with multiple admissions for chest infections. Given her family history and high clinical suspicion, a diagnosis of Griscelli syndrome and hemophagocytic lymphohistiocytosis was made. Her work-up included a brain
Externí odkaz:
https://doaj.org/article/dc7866a04503483ca62871753c213edb
Publikováno v:
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 441-443 (2019)
We encountered an extremely rare case where a patient with cat eye syndrome (CES) who presented with symptoms of posterior semicircular canal dehiscence (PSCD). CES is a rare genetic disorder, resulting from duplication of chromosome 22. Patients may
Externí odkaz:
https://doaj.org/article/6cd277871eaf4dad8187a88682809e18
Autor:
Ali Mir, Montaha AlMudhry, Wajd AlOtaibi, Rami AlHazmi, Raidah AlBaradie, Qasim AlHarbi, Shahid Bashir, Omar Chamdine, Yousef Housawi
Publikováno v:
Journal of Pediatric Hematology/Oncology.
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 429-433 (2021)
Case Reports in Neurology
Case Reports in Neurology
MEGDEL 3-methylglutaconic (MG) aciduria, deafness, encephalopathy, Leigh-like syndrome is an autosomal recessive disorder associated with infantile hypoglycemia, progressive psychomotor developmental delay, cerebellar atrophy with lesions in the basa
Publikováno v:
Radiology Case Reports, Vol 15, Iss 11, Pp 2339-2342 (2020)
Radiology Case Reports
Radiology Case Reports
Our case involved a 1-year-old female with multiple admissions for chest infections. Given her family history and high clinical suspicion, a diagnosis of Griscelli syndrome and hemophagocytic lymphohistiocytosis was made. Her work-up included a brain
Publikováno v:
Neurosciences (Riyadh, Saudi Arabia). 26(4)
Objective: Invasive aspergillosis of the central nervous system in immunocompetent patients is a rare disease. We present in this study three cases that were treated in our centre and reviewed the results of similar studies from Saudi Arabia. Methods
Publikováno v:
Annals of Saudi Medicine
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 441-443 (2019)
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 441-443 (2019)
We encountered an extremely rare case where a patient with cat eye syndrome (CES) who presented with symptoms of posterior semicircular canal dehiscence (PSCD). CES is a rare genetic disorder, resulting from duplication of chromosome 22. Patients may