Results 151 to 160 of about 4,530 (250)

Different Neuronal Networks Are Associated with Spikes and Slow Activity in Hypsarrhythmia

, 2007
Michael Siniatchkin, Andreas van Baalen, Julia Jacobs, Friederike Moeller, Jan Moehring, Rainer Boor, Stephan Wolff, Olav Jansen, Ulrich Stephani   +8 more
openalex   +1 more source

Teaching Neuro Images : Infant with glutaric aciduria type 1 presenting with infantile spasms and hypsarrhythmia [PDF]

, 2013
N. Young‐Lin, Sarah Shalev, Orit A. Glenn, Marisa Gardner, Chung Lee, Anthony Wynshaw‐Boris, Amy A. Gelfand   +6 more
openalex   +1 more source

An Unusual Presentation of Infantile Epileptic Spasm Syndrome in a Child. [PDF]

Turk Arch Pediatr
Yıldırım M, Akyol Özkara K, Çiçek S, Bektaş Ö, Teber S.   +4 more
europepmc   +1 more source

Role of the Ketogenic Diet Therapy and ACTH as Second Treatments in Drug-Resistant Infantile Epileptic Spasms Syndrome. [PDF]

Nutrients
Dressler A, Bonfanti L, Trimmel-Schwahofer P, Porsche B, Bertoli S, Male C.   +5 more
europepmc   +1 more source

MECP2 duplication syndrome-Typical EEG characteristics. [PDF]

Epileptic Disord
Otu W, Sudhakaran R, Garza-Garcia G, Parekh K, Sheikh IS.   +4 more
europepmc   +1 more source

Phenotypic Spectrum of STXBP1 Gene Mutations in an Emirati Case Series. [PDF]

Cureus, 2023
Pawar N, Farid Mir F, Tahir S, Kashyape P, Babiker MOE.   +4 more
europepmc   +1 more source

A rare cause of epileptic encephalopathy: case report of a novel patient with PEHO-like phenotype and CCDC88A gene pathogenic variants. [PDF]

Ital J Pediatr
Papuc SM, Glangher A, Erbescu A, Arsene OT, Arghir A, Budisteanu M.   +5 more
europepmc   +1 more source

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases

, 2011
Uluç Yiş, Semra Hız Kurul, Özden Anal, Eray Dırık   +3 more
openalex   +2 more sources

The Oral Findings and Dental Management of Patients with West Syndrome: A Case Series and Literature Review. [PDF]

J Clin Med
Limeres-Posse J, Muñoz-Navarro C, García-Mato E, Sande-López L, Diniz-Freitas M, Diz-Dios P, Rivas-Mundiña B.   +6 more
europepmc   +1 more source

Mixed Segmental Uniparental Disomy of Chromosome 15q11-q1 Coexists with Homozygous Variant in <i>GNB5</i> Gene in Child with Prader-Willi and Lodder-Merla Syndrome. [PDF]

Genes (Basel)
Marczyk T, Libura M, Wikiera B, Góralska M, Pollak A, Telenga M, Płoski R, Śmigiel R.   +7 more
europepmc   +1 more source