Results 31 to 40 of about 638,325 (347)

"Electro-clinical Syndromes" with onset in Paediatric Age. the highlights of the clinical-EEG, genetic and therapeutic advances [PDF]

, 2011
The genetic causes underlying epilepsy remain largely unknown, and the impact of available genetic data on the nosology of epilepsy is still limited.
Alberto Verrotti, CASTALDO, Rosa, FERRETTI, ALESSANDRO, Filomena Ianniello, Francesco Chiarelli, PAOLINO, MARIA CHIARA, PARISI, Pasquale, VILLA, MARIA PIA   +7 more
core   +2 more sources

Valproate for Intractable Epilepsy

Pediatric Neurology Briefs, 1992
The efficacy and side effects of high dose valproic acid (VPA) therapy in 46 children with refractory epilepsy were studied at the Department of Child Neurology, Okayama University Medical School, Okayama, Japan.
J Gordon Millichap
doaj   +1 more source

Epidemiological associations between brachycephaly and upper respiratory tract disorders in dogs attending veterinary practices in England [PDF]

, 2015
Background: Brachycephalic dog breeds are increasingly common. Canine brachycephaly has been associated with upper respiratory tract (URT) disorders but reliable prevalence data remain lacking.
AG Drake, AJ German, AK Hussein, Anon, BR Kirkwood, C Rusbridge, CD Knecht, CV Torrez, D Alderton, D Aron, D Bannasch, D Georgevsky, D Lorenzi De, DA Koch, DG O’Neill, DG O’Neill, DG O’Neill, DN Irion, EM Lund, F Bernaerts, FJ Fasanella, FS Roedler, HG Parker, I Dohoo, J Clutton-Brock, J Sampson, JJ Schoenebeck, JJ Schoenebeck, K Lindblad-Toh, L Asher, LM Collins, MJ Schmidt, MW Neff, NJ Beausoleil, P Bateson, PD McGreevy, RMA Packer, S Fonfara, S Isono, T Emmerson   +39 more
core   +2 more sources

Neuro-developmental and epilepsy outcomes of children with west syndrome: A cross-sectional study from North India

Annals of Indian Academy of Neurology, 2020
Objectives: To assess the neurodevelopmental outcome of West syndrome (WS) in Indian children, who differ in their clinical profile from the western population.
Juhi Gupta, Suvasini Sharma, Sharmila B Mukherjee, Puneet Jain, Satinder Aneja   +4 more
doaj   +1 more source

Rett Syndrome: Revised diagnostic criteria and nomenclature [PDF]

, 2010
Objective: Rett syndrome (RTT) is a severe neurodevelopmental disease that affects approximately 1 in 10,000 live female births and is often caused by mutations in Methyl-CpG-binding protein 2 (MECP2). Despite distinct clinical features, the accumulation
Amir, Archer, Ariani, Artuso, Bahi-Buisson, Carney, Christen, Einspieler, Goutieres, Hagberg, Hagberg, Hagberg, Hagberg, Hanefeld, Huppke, Kankirawatana, Leonard, Neul, Percy, Renieri, Rett, Rolando, Wan, Watson, Zappella   +24 more
core   +1 more source

The early electroclinical manifestations of infantile spasms: A video EEG study

Annals of Indian Academy of Neurology, 2016
Purpose: Infantile spasms are described as flexor extensor and mixed; but more features of their semiology and ictal electroencephalography (EEG) changes are sparse in the literature.
Mary Iype, Puthuvathra Abdul Mohammed Kunju, Geetha Saradakutty, Devi Mohan, Shahanaz Ahamed Mohammed Khan   +4 more
doaj   +1 more source

Current ecological understanding of fungal-like pathogens of fish: what lies beneath? [PDF]

, 2014
Despite increasingly sophisticated microbiological techniques, and long after the first discovery of microbes, basic knowledge is still lacking to fully appreciate the ecological importance of microbial parasites in fish. This is likely due to the nature
Casey eJessop, Demetra eAndreou, Frank H Gleason, Osu eLilje, Rodolphe Elie Gozlan, Rodolphe Elie Gozlan, Wyth eMarshall   +6 more
core   +4 more sources

BLM and RMI1 alleviate RPA inhibition of topoIIIα decatenase activity [PDF]

, 2012
RPA is a single-stranded DNA binding protein that physically associates with the BLM complex. RPA stimulates BLM helicase activity as well as the double Holliday junction dissolution activity of the BLM-topoisomerase IIIα complex.
A Bochkarev, A Machwe, AR Meetei, C Iftode, CF Chen, Csanad Z. Bachrati, CZ Bachrati, D Sikder, D Xu, Grant W. Brown, H Goulaouic, Ian D. Hickson, ID Hickson, J Yang, J Yin, Jay Yang, JJ Champoux, JL Plank, JL Plank, K Kirkegaard, KM Doherty, L Wu, L Wu, MP Fairman, MS Wold, MS Wold, NA Desai, NA Ellis, P Cejka, P Mohaghegh, PL Garcia, RM Brosh Jr, RS Chaganti, S Raynard, S Raynard, S Sharma, Sergey Korolev, T Wechsler, Y Liu, Y Zou   +39 more
core   +16 more sources

A unique collaborative model providing supportive and self-advocacy tools to the rare disease community

Rare
The National Ehlers-Danlos Syndromes (EDS) service is a highly specialised NHS commissioned service for diagnosing and supporting people with a rare, monogenic type of EDS.
Juliette M. Harris, Jacqui Fish, Jared Griffin, Gemma Hasnaoui, Clare Stacey, Neeti Ghali, Fleur S. van Dijk   +6 more
doaj   +1 more source

Autism, the Integrations of 'Difference' and the Origins of Modern Human Behaviour [PDF]

, 2009
It is proposed here that the archaeological evidence for the emergence of 'modern behaviour' (160,000-40,000 bp) can best be explained as the rise of cognitive variation within populations through social mechanisms for integrating 'different minds ...
Spikins, Penny
core   +1 more source