Results 241 to 250 of about 447,569 (400)

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source

Moderate hypothermia to treat perinatal asphyxial encephalopathy.

New England Journal of Medicine, 2009
D. Azzopardi, B. Strohm, A. Edwards, L. Dyet, H. Halliday, E. Juszczak, O. Kapellou, M. Levene, N. Marlow, E. Porter, M. Thoresen, A. Whitelaw, P. Brocklehurst   +12 more
semanticscholar   +1 more source

Iron Encephalopathy [PDF]

BMJ, 1951
C A, BIRCH, M, TILL
openaire   +2 more sources

Silent toxicity: A rare case of 5-fluorouracil-induced hyperammonemic encephalopathy. [PDF]

Oncoscience
Kalfoutzou A, Rapti C, Bagiokou E, Kolintzikis V, Ramfidis V.   +4 more
europepmc   +1 more source

Precision therapies for genetic epilepsies in 2025: Promises and pitfalls

Epilepsia Open, EarlyView.
Abstract By targeting the underlying etiology, precision therapies offer an exciting paradigm shift to improve the stagnant outcomes of drug‐resistant epilepsies, including developmental and epileptic encephalopathies. Unlike conventional antiseizure medications (ASMs) which only treat the symptoms (seizures) but have no effect on the underlying ...
Shuyu Wang, Emilio Perucca, Samuel F. Berkovic, Piero Perucca   +3 more
wiley   +1 more source

Effect of non–invasive ventilation on central and brain hemodynamics in term newborn infants with hypoxic – ischemic encephalopathy

, 2020
Elena Klevakina, І. О. Анікін, І. О. Анікін, Olexandr Mykhalchuk, Olexandr Mykhalchuk   +4 more
openalex   +2 more sources

Comparative studies on the thermostability of five strains of transmissible-spongiform-encephalopathy agent [PDF]

, 2007
Fernie, Karen, Somerville, Robert A, Steele, P J, Taylor, D M   +3 more
core   +1 more source

Acute leukoencephalopathy with restricted diffusion (ALERD) in a toddler: A diagnostic challenge unmasking hereditary sensory autonomic neuropathy type 4. [PDF]

BMJ Case Rep
Gowda VK, Varghese A, Kinhal UV, Srinivasan VM, Nayyer A.   +4 more
europepmc   +1 more source

From mechanism to phenotype: What fits in a basket trial

Epilepsia, EarlyView.
Kette D. Valente
wiley   +1 more source

Absence seizures: Update on signaling mechanisms and networks

Epilepsia Open, EarlyView.
Abstract Absence seizures (AS) are a hallmark of genetic generalized epilepsies (GGE), characterized by brief episodes of impaired consciousness accompanied by electroencephalographic spike‐and‐wave discharges (SWDs). Traditionally attributed to cortico‐thalamo‐cortical (CTC) dysrhythmia, emerging evidence suggests a more intricate pathophysiological ...
Ozlem Akman, Filiz Onat
wiley   +1 more source