Results 1 - 10 of 20 for General Search
Show only
Refined by:
collection:
Wiley Online Library All Journals
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
|
|
A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxiaAl Tassan, Nada ; Khalil, Dania ; Shinwari, Jameela ; Al Sharif, Latifa ; Bavi, Prashant ; Abduljaleel, Zainularifeen ; Abu Dhaim, Nada ; Magrashi, Amna ; Bobis, Steve ; Ahmed, Hala ; AlAhmed, Samaher ; Bohlega, SaeedHuman mutation, 2012-02, Vol.33 (2), p.351-354 [Peer Reviewed Journal]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyFull text available |
| 2 |
Material Type: Article
|
|
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosisAl-Saif, Amr ; Al-Mohanna, Futwan ; Bohlega, SaeedAnnals of neurology, 2011-12, Vol.70 (6), p.913-919 [Peer Reviewed Journal]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyFull text available |
| 3 |
Material Type: Article
|
|
Autosomal-recessive syndrome with alopecia, hypadism, progressive extra- pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1Al-Semari, Abdulaziz ; Bohlega, SaeedAmerican journal of medical genetics. Part A, 2007-01, Vol.143A (2), p.149-160 [Peer Reviewed Journal]Full text available |
| 4 |
Material Type: Article
|
|
Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1Al-Semari, Abdulaziz ; Bohlega, SaeedAmerican journal of medical genetics. Part A, 2007-01, Vol.143A (2), p.149-160 [Peer Reviewed Journal]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyFull text available |
| 5 |
Material Type: Article
|
|
Cerebrotendinous xanthomatosis: A candidate for ACMG list of secondary findings?Khouj, Ebtissal ; Bohlega, Saeed ; Alkuraya, Fowzan S.Clinical genetics, 2023-01, Vol.103 (1), p.125-126 [Peer Reviewed Journal]Oxford, UK: Blackwell Publishing LtdFull text available |
| 6 |
Material Type: Article
|
|
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsulaBohlega, Saeed ; Al-Jishi, Adel ; Dobson-Stone, Carol ; Rampoldi, Luca ; Saha, Parthasarathi ; Murad, Hatem ; Kareem, Abid ; Roberts, George ; Monaco, Anthony P.Movement disorders, 2003-04, Vol.18 (4), p.403-407 [Peer Reviewed Journal]New York: Wiley Subscription Services, Inc., A Wiley CompanyFull text available |
| 7 |
Material Type: Article
|
|
Dissecting the Phenotype and Genotype of PLA2G6‐Related ParkinsonismMagrinelli, Francesca ; Mehta, Sahil ; Di Lazzaro, Giulia ; Latorre, Anna ; Edwards, Mark J. ; Balint, Bettina ; Basu, Purba ; Kobylecki, Christopher ; Groppa, Sergiu ; Hegde, Anaita ; Mulroy, Eoin ; Estevez‐Fraga, Carlos ; Arora, Anshita ; Kumar, Hrishikesh ; Schneider, Susanne A. ; Lewis, Patrick A. ; Jaunmuktane, Zane ; Revesz, Tamas ; Gandhi, Sonia ; Wood, Nicholas W. ; Hardy, John A. ; Tinazzi, Michele ; Lal, Vivek ; Houlden, Henry ; Bhatia, Kailash P.Movement disorders, 2022-01, Vol.37 (1), p.148-161 [Peer Reviewed Journal]Hoboken, USA: John Wiley & Sons, IncFull text available |
| 8 |
Material Type: Article
|
|
Expert opinion on clinical experience with subcutaneous interferon beta‐1a in multiple sclerosis patients with different disease activity profilesBohlega, Saeed ; Alroughani, Raed ; Alkhawajah, Mona ; Alsaadi, Taoufik ; Daif, Abdulkader ; Elalamy, Osama R. ; Inshasi, Jihad S. ; Noori, Suzan ; Shakra, Mustafa ; Shatila, Ahmed O. ; Boghdady, Ahmed El ; Boshra, AmirNeurology and clinical neuroscience, 2019-09, Vol.7 (5), p.260-266 [Peer Reviewed Journal]Tokyo: Wiley Subscription Services, IncFull text available |
| 9 |
Material Type: Article
|
|
Gastrointestinal involvement in neuromuscular disordersFinsterer, Josef ; Strobl, WalterJournal of gastroenterology and hepatology, 2024-06 [Peer Reviewed Journal]Full text available |
| 10 |
Material Type: Article
|
|
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsyMinassian, Berge A. ; Sainz, Jesus ; Serratosa, Jose M. ; Gee, Manyee ; Sakamoto, Lise M. ; Bohlega, Saeed ; Geoffroy, Guy ; Barr, Cathy ; Scherer, Steve W. ; Tomiyasu, Uwamie ; Carpenter, Stirling ; Wigg, Karen ; Sanghvi, A. V. ; Delgado-Escueta, Antonio V.Annals of neurology, 1999-02, Vol.45 (2), p.262-265 [Peer Reviewed Journal]New York: John Wiley & Sons, IncFull text available |
Results 1 - 10 of 20 for General Search
Personalize your results
Refine Search Results
Expand My Results
Show only
Subject
- Life Sciences & Biomedicine (16)
- Science & Technology (16)
- Humans (12)
- Clinical Neurology (11)
- Neurosciences & Neurology (11)
- Magnetic Resonance Imaging (8)
- Female (8)
- Male (8)
- Medical Sciences (8)
- Biological And Medical Sciences (8)
- Neurosciences (6)
- Neurology (6)
- Pedigree (5)
- Adolescent (5)
- Brain - Pathology (4)
- Child (4)
- Genotype (3)
- Genetics & Heredity (3)
- Dystonia (3)
- Adult (3)
-
More options
Creation Date
- Before1998 (4)
- 1998To2002 (5)
- 2003To2006 (3)
- 2007To2019 (6)
- After 2019 (3)
-
More options
Database/Library
- Wiley Online Library Journals (20)
- Journals@Ovid Full Text (19)
- Wiley-Blackwell Full Collection 2013 (19)
- Wiley Online Library (19)
- Science Citation Index Expanded (Web of Science) (14)
- MEDLINE Complete (EBSCOhost) (8)
- Wiley-Blackwell Open Access Collection (6)
- Publisher or Other Site (5)
- Wiley-Blackwell Full Collection 2009 (5)
- Academic Search Premier (1)
- EZB* (1)
- Open Access: Hindawi Publishing (1)
-
More options
Journal Title
- Annals Of Neurology (4)
- Movement Disorders (4)
- Muscle & Nerve (2)
- American Journal Of Medical Genetics. Part A (2)
- European Journal Of Neurology (2)
- Human Mutation (1)
- Journal Of Gastroenterology And Hepatology (1)
- Clinical Genetics (1)
- Neurology And Clinical Neuroscience (1)
- Cancer (1)
-
More options
Home Page
RSS
Feed
Policies
Contact Us-
Implemented by:
Social Network Logos: 