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11
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease
Material Type:
Artículo
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Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease

Yemni, Eman Al ; Monies, Dorota ; Alkhairallah, Thamer ; Bohlega, Saeed ; Abouelhoda, Mohamed ; Magrashi, Amna ; Mustafa, Abeer ; AlAbdulaziz, Basma ; Alhamed, Mohamed ; Baz, Batoul ; Goljan, Ewa ; Albar, Renad ; Jabaan, Amjad ; Faquih, Tariq ; Subhani, Shazia ; Ali, Wafa ; Shinwari, Jameela ; Al-Mubarak, Bashayer ; Al-Tassan, Nada

Scientific reports, 2019-03, Vol.9 (1), p.3344-3344, Article 3344 [Revista revisada por pares]

England: Nature Publishing Group

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12
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity
Material Type:
Artículo
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Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity

Dressler, Dirk ; Altavista, Maria Concetta ; Altenmueller, Eckart ; Bhidayasiri, Roongroj ; Bohlega, Saeed ; Chana, Pedro ; Chung, Tae Mo ; Colosimo, Carlo ; Fheodoroff, Klemens ; Garcia-Ruiz, Pedro J. ; Jeon, Beomseok ; Jin, Lingjing ; Kanovsky, Petr ; Milanov, Ivan ; Micheli, Federico ; Orlova, Olga ; Pandey, Sanjay ; Pirtosek, Zvezdan ; Relja, Maja ; Rosales, Raymond ; Sagástegui-Rodríguez, José Alberto ; Shahidi, Gholam Ali ; Timerbaeva, Sofia ; Wan, Xinhua ; Walter, Uwe ; Saberi, Fereshte Adib

Journal of Neural Transmission, 2021-03, Vol.128 (3), p.321-335 [Revista revisada por pares]

Vienna: Springer Vienna

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13
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalation
Material Type:
Artículo
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Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalation

B Mohammed, Walaa ; Tarabzouni, Salma ; Bohlega, Saeed

BMJ neurology open, 2022-05, Vol.4 (1), p.e000221-e000221 [Revista revisada por pares]

England: BMJ Publishing Group Ltd

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14
Novel mutation of the notch3 gene in arabic family with CADASIL
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Artículo
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Novel mutation of the notch3 gene in arabic family with CADASIL

Bohlega, Saeed

Neurology international, 2011-07, Vol.3 (2), p.e6-e6 [Revista revisada por pares]

Italy: MDPI AG

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15
Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia
Material Type:
Artículo
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Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia

Alharbi, Norah ; Matar, Rawan ; Cupler, Edward ; Al-Hindi, Hindi ; Murad, Hatem ; Alhomud, Iftteah ; Monies, Dorota ; Alshehri, Ali ; Alyahya, Mossaed ; Meyer, Brian ; Bohlega, Saeed

Frontiers in neuroscience, 2022-02, Vol.16, p.815556-815556 [Revista revisada por pares]

Switzerland: Frontiers Research Foundation

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16
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
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Artículo
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Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

Wakil, Salma M ; Alhissi, Safa ; Al Dossari, Haya ; Alqahtani, Ayesha ; Shibin, Sherin ; Melaiki, Brahim T ; Finsterer, Josef ; Al-Hashem, Amal ; Bohlega, Saeed ; Alazami, Anas M

BMC medical genetics, 2019-07, Vol.20 (1), p.119-119, Article 119 [Revista revisada por pares]

England: BioMed Central Ltd

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17
Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi Arabia
Material Type:
Artículo
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Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi Arabia

Alharbi, Norah ; Bohlega, Saeed ; Alhindi, Hindi ; Matar, Rawan

Journal of the neurological sciences, 2023-12, Vol.455, p.122521, Article 122521 [Revista revisada por pares]

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18
Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)
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Artículo
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Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)

Abusrair, Ali ; Bohlega, Saeed

Neurology, 2019-04, Vol.92 (15_supplement) [Revista revisada por pares]

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19
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
Material Type:
Artículo
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LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

BOHLEGA, SAEED A. ; ALFAWAZ, SARAH ; ABOU-AL-SHAAR, HUSSAM ; AL-HINDI, HINDI N. ; MURAD, HATEM N. ; BOHLEGA, MOHAMED S. ; MEYER, BRIAN F. ; MONIES, DOROTA

Acta myologica, 2018-09, Vol.37 (3), p.221-226 [Revista revisada por pares]

Pacini Editore srl

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20
Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review
Material Type:
Artículo
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Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review

AlSharoqi, Isa Ahmed ; Aljumah, Mohamed ; Bohlega, Saeed ; Boz, Cavit ; Daif, Abdelkader ; El-Koussa, Salam ; Inshasi, Jihad ; Kurtuncu, Murat ; Müller, Thomas ; Retief, Chris ; Sahraian, Mohammad Ali ; Shaygannejad, Vahid ; Slassi, Ilham ; Taha, Karim ; Zakaria, Magd ; Sørensen, Per Soelberg

Neurology and therapy, 2020-06, Vol.9 (1), p.55-66 [Revista revisada por pares]

Cheshire: Springer Healthcare

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