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Multiparametric cerebellar imaging and clinical phenotype in childhood ataxia telangiectasia. [electronic resource] by
- Dineen, Rob A
- Raschke, Felix
- McGlashan, Hannah L
- Pszczolkowski, Stefan
- Hack, Lorna
- Cooper, Andrew D
- Prasad, Manish
- Chow, Gabriel
- Whitehouse, William P
- Auer, Dorothee P
Producer: 20210111
In:
NeuroImage. Clinical vol. 25
Availability: No items available.
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16.
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Neurological manifestations of influenza infection in children and adults: results of a National British Surveillance Study. [electronic resource] by
- Goenka, Anu
- Michael, Benedict D
- Ledger, Elizabeth
- Hart, Ian J
- Absoud, Michael
- Chow, Gabriel
- Lilleker, James
- Lunn, Michael
- McKee, David
- Peake, Deirdre
- Pysden, Karen
- Roberts, Mark
- Carrol, Enitan D
- Lim, Ming
- Avula, Shivaram
- Solomon, Tom
- Kneen, Rachel
Producer: 20141217
In:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America vol. 58
Availability: No items available.
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17.
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Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya. [electronic resource] by
- Tho-Calvi, Sara C
- Thompson, Dominic
- Saunders, Dawn
- Agrawal, Shakti
- Basu, Anna
- Chitre, Manali
- Chow, Gabriel
- Gibbon, Frances
- Hart, Anthony
- Tallur, Krishnaraya Kamath
- Kirkham, Fenella
- Kneen, Rachel
- McCullagh, Helen
- Mewasingh, Leena
- Vassallo, Grace
- Vijayakumar, Kayal
- Wraige, Elizabeth
- Yeo, Tong Hong
- Ganesan, Vijeya
Producer: 20190723
In:
Neurology vol. 90
Availability: No items available.
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18.
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Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. [electronic resource] by
- Geranmayeh, Fatemeh
- Clement, Emma
- Feng, Lucy H
- Sewry, Caroline
- Pagan, Judith
- Mein, Rachael
- Abbs, Stephen
- Brueton, Louise
- Childs, Anne-Marie
- Jungbluth, Heinz
- De Goede, Christian G
- Lynch, Bryan
- Lin, Jean-Pierre
- Chow, Gabriel
- Sousa, Carlos de
- O'Mahony, Olivia
- Majumdar, Anirban
- Straub, Volker
- Bushby, Katherine
- Muntoni, Francesco
Producer: 20100729
In:
Neuromuscular disorders : NMD vol. 20
Availability: No items available.
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19.
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Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. [electronic resource] by
- Logan, Clare V
- Cossins, Judith
- Rodríguez Cruz, Pedro M
- Parry, David A
- Maxwell, Susan
- Martínez-Martínez, Pilar
- Riepsaame, Joey
- Abdelhamed, Zakia A
- Lake, Alice V R
- Moran, Maria
- Robb, Stephanie
- Chow, Gabriel
- Sewry, Caroline
- Hopkins, Philip M
- Sheridan, Eamonn
- Jayawant, Sandeep
- Palace, Jacqueline
- Johnson, Colin A
- Beeson, David
Producer: 20160322
In:
American journal of human genetics vol. 97
Availability: No items available.
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20.
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The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. [electronic resource] by
- Rodríguez Cruz, Pedro M
- Cossins, Judith
- Estephan, Eduardo de Paula
- Munell, Francina
- Selby, Kathryn
- Hirano, Michio
- Maroofin, Reza
- Mehrjardi, Mohammad Yahya Vahidi
- Chow, Gabriel
- Carr, Aisling
- Manzur, Adnan
- Robb, Stephanie
- Munot, Pinki
- Wei Liu, Wei
- Banka, Siddharth
- Fraser, Harry
- De Goede, Christian
- Zanoteli, Edmar
- Conti Reed, Umbertina
- Sage, Abigail
- Gratacos, Margarida
- Macaya, Alfons
- Dusl, Marina
- Senderek, Jan
- Töpf, Ana
- Hofer, Monika
- Knight, Ravi
- Ramdas, Sithara
- Jayawant, Sandeep
- Lochmüller, Hans
- Palace, Jacqueline
- Beeson, David
Producer: 20200312
In:
Brain : a journal of neurology vol. 142
Availability: No items available.
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