1. A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.
Gribaa M, Salih M, Anheim M, Lagier-Tourenne C, H'mida D, Drouot N, Mohamed A, Elmalik S, Kabiraj M, Al-Rayess M, Almubarak M, Bétard C, Goebel H, Koenig M.
Brain. 2007 Jul;130(Pt 7):1921-8. Epub 2007 Apr 30.
PMID:17470496[PubMed - indexed for MEDLINE] Free Article
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2. C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy.
Carmignac V, Salih MA, Quijano-Roy S, Marchand S, Al Rayess M, Mukhtar MM, Urtizberea JA, Labeit S, Guicheney P, Leturcq F, Gautel M, Fardeau M, Campbell KP, Richard I, Estournet B, Ferreiro A.
Ann Neurol. 2007 Apr;61(4):340-51.
PMID:17444505[PubMed - indexed for MEDLINE]
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3. Stroke due to mitochondrial disorders in Saudi children.
Salih MA, Abdel-Gader AG, Zahraa JN, Al-Rayess M, Alorainy IA, Hassan HH, Ruitenbeek W, Zeviani M.
Saudi Med J. 2006 Mar;27 Suppl 1:S81-90.
PMID:16532135[PubMed - indexed for MEDLINE]
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4. Brain metastasis as an initial manifestation of a gallbladder carcinoma.
Joel R JR Tayo, Huda H Al-Abdulkarim, and Molham M Al-Rayess
Neurosciences (Riyadh) 10(3):235-7 (2005),
PMID 22473267
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5. Morphologic patterns of male infertility in Saudi patients. A University Hospital experience.
Al-Rayess M, Al-Rikabi AC.
Saudi Med J. 2000 Jul;21(7):625-8.
PMID:11500724[PubMed - indexed for MEDLINE]
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6. Prevalence of intratubular germ cell neoplasia of the testis.
Riyadh F. Talic, Al-Rikabi AC, Al-Rayess M.
Saudi Med J. 1999; Vol. 20(9):706-710.
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7. Intramedullary ossified cavernous angioma of the spinal cord: case report.
Naim-Ur-Rahman, Jamjoom A, Al-Rayess M.
Br J Neurosurg. 1998 Jun;12(3):267-70.
PMID:11013693[PubMed - indexed for MEDLINE]
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8. Intraventricular and leptomeningeal dissemination of a pilocytic cerebellar astrocytoma in a child with a ventriculoperitoneal shunt: case report.
Jamjoom AB, Jamjoom ZA, Al-Rayess M.
Br J Neurosurg. 1998 Feb;12(1):56-8.
PMID:11013652[PubMed - indexed for MEDLINE]
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9. Cerebellopontine angle medulloblastoma.
Naim-ur-Rahman, Jamjoom A, Al-Rayess M, Jamjoom ZA.
Br J Neurosurg. 2000 Jun;14(3):262-3. No abstract available.
PMID:10912209[PubMed - indexed for MEDLINE]
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10. Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity.
Salih MA, Maisonobe T, Kabiraj M, Al Rayess M, al-Turaiki MH, Akbar M, Tahan A, Urtizberea JA, Grid D, Hamadouche T, Guilbot A, Brice A, Leguern E.
Neuromuscul Disord. 2000 Jan;10(1):10-5.
PMID:10677858[PubMed - indexed for MEDLINE]
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11. A novel form of familial congenital muscular dystrophy in two adolescents.
Salih MA, Al Rayess M, Cutshall S, Urtizberea JA, Al-Turaiki MH, Ozo CO, Straub V, Akbar M, Abid M, Andeejani A, Campbell KP.
Neuropediatrics. 1998 Dec;29(6):289-93.
PMID:10029346[PubMed - indexed for MEDLINE]
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12. Metastatic deposits of a high-grade malignant glioma in cervical lymph nodes diagnosed by fine needle aspiration (FNA) cytology--case report and literature review.
al-Rikabi AC, al-Sohaibani MO, Jamjoom A, Al-Rayess M.
Cytopathology. 1997 Dec;8(6):421-7. Review. No abstract available.
PMID:9439895[PubMed - indexed for MEDLINE]
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13. Giant cell arteritis: Report of two Saudi patients and review of the literature.
Al Tahan A, Al Rayess M, Abduljabbar M, Al Moallem M.
Ann Saudi Med. 1997 Mar;17(2):237-9. No abstract available.
PMID:17377441[PubMed - in process]
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14. Axonal dystrophy presenting as the megacystis-microcolon-intestinal hypoperistalsis syndrome.
Al-Rayess M, Ambler MW.
Pediatr Pathol. 1992 Sep-Oct;12(5):743-50.
PMID:1437888[PubMed - indexed for MEDLINE]
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15. Spectroscopic imaging of stroke in humans: histopathology correlates of spectral changes.
Petroff OA, Graham GD, Blamire AM, Al-Rayess M, Rothman DL, Fayad PB, Brass LM, Shulman RG, Prichard JW.
Neurology. 1992 Jul;42(7):1349-54.
PMID:1620345[PubMed - indexed for MEDLINE]
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16. Dysplasia of the corpus callosum in identical twins with nonketotic hyperglycinemia.
Rogers T, Al-Rayess M, O'Shea P, Ambler MW.
Pediatr Pathol. 1991 Nov-Dec;11(6):897-902.
PMID:1775403[PubMed - indexed for MEDLINE]