Results 191 to 200 of about 322,048 (294)

Acute Neurological Events in Children With Hemoglobin SC Disease: A Multicenter Retrospective Study

Pediatric Blood &Cancer, Volume 73, Issue 11, November 2026.
ABSTRACT Introduction Neurological manifestations in children with hemoglobin SC (HbSC) disease remain insufficiently characterized, particularly regarding acute events. The aim of this study was to describe the spectrum and frequency of acute neurological events in a multicenter cohort of children with HbSC disease.
Célia Paulmin, Bérengère Koehl, Audrey Maudoux, Hanine Mansour, Marie‐Hélène Odievre, Nathalie Garrec, Emilie Georget, Cécile Arnaud, Slimane Allali, Lydia Doumdo, Marie Belloy, Corinne Guitton   +11 more
wiley   +1 more source

Extended release huperzine for the treatment of idiopathic epilepsy in dogs - a Case Report. [PDF]

Front Vet Sci
Grant KL, Long SN.
europepmc   +1 more source

High‐Resolution IVIM MRI Characterizes Diffusion–Perfusion Properties of the Parasagittal Dura

NMR in Biomedicine, Volume 39, Issue 11, November 2026.
Parasagittal dura demonstrates intermediate diffusion and elevated perfusion‐related IVIM metrics compared with brain parenchyma, reflecting its unique microfluidic environment at the CSF–dura interface. IVIM imaging of the parasagittal dura provides a rapid, noncontrast MRI approach to assess dural fluid transport and may offer a potential imaging ...
Yi‐Jui Liu, Chun‐Han Liao, Shin‐Lei Peng, Shao‐Chieh Lin, Chao‐Chun Lin, Chia‐Wei Lin, Chia‐Hong Hsieh, Chun‐Wen Chen, Hing‐Chiu Chang   +8 more
wiley   +1 more source

Cerebrospinal fluid-specific oligoclonal bands in dogs with idiopathic epilepsy. [PDF]

J Vet Intern Med
Föhr J, Prümmer JK, Maiolini A, Marti E, Jelcic I, Vidondo B, Ziegler M, Bathen-Nöthen A, Tipold A, Volk HA, Stein VM.   +10 more
europepmc   +1 more source

Case Report on Acquired Hepatocerebral Degeneration

Progress in Neurology and Psychiatry, Volume 30, Issue 4, November 2026.
ABSTRACT Acquired hepatocerebral degeneration (AHD) is an uncommon neurological manifestation of chronic liver disease, most often associated with portosystemic shunting. The disorder is characterised by a combination of movement abnormalities, cognitive decline, and psychiatric disturbance. Manganese accumulation within the basal ganglia, secondary to
Aamir Khan, Odai Jumma, Taram Nayab
wiley   +1 more source

Exploring Gut Microbiota-Targeted Therapies for Canine Idiopathic Epilepsy. [PDF]

Int J Mol Sci
Blanquet L, Serra D, Marrinhas C, Almeida A.   +3 more
europepmc   +1 more source

Suspected hyperthyroidism‐associated myoclonus in a cat

Veterinary Record Case Reports, Volume 14, Issue 4, November 2026.
Abstract A 10‐year‐old, male, neutered domestic shorthair cat presented with a 2‐week history of progressively worsening myoclonic jerks predominantly involving the head. Jerks were continuous and marked at rest, but became less intense during activity.
Magdalena Maria Dyrka, Ian Ramsey, Fiona May Keir James, Grace Kadler, Jessica Zilli, Rodrigo Gutierrez Quintana   +5 more
wiley   +1 more source

An Exploratory Study on the Relationship Between Idiopathic Epilepsy and Sleep in Dogs. [PDF]

J Vet Intern Med
Mondino A, Nettifee J, Muñana KR.
europepmc   +1 more source

Corticosteroid‐augmented interfascial injections for cancer pain management in a dog

Veterinary Record Case Reports, Volume 14, Issue 4, November 2026.
Abstract A 9‐year‐old Rottweiler with metastatic osteosarcoma developed severe episodic pain following forelimb amputation and progression of neoplastic disease. Despite extensive multimodal systemic analgesia, including NSAIDs, gabapentin, amantadine and later amitriptyline, the dog showed persistent vocalisation and touch‐evoked pain in the axillary ...
Zita Julianna Szabo, Simona Vincenti, Mariateresa Camerino, Isabelle Iff   +3 more
wiley   +1 more source

Clinical and genetic characterization of intellectual disability

Developmental Medicine &Child Neurology, Volume 68, Issue 11, Page 1601-1609, November 2026.
This study examines the etiological factors and comorbidities in a large cohort of Finnish patients with intellectual disability. Genetic causes—including chromosomal abnormalities and pathogenic gene variants—were more frequently identified in individuals with moderate to profound intellectual disability.
Aarni Venetvaara, Minna Kraatari‐Tiri, Jussi‐Pekka Tolonen, Marko Merikukka, IDGEN Study Group, Hannaleena Kokkonen, Teija Paakkola, Susanna Varis, Antti Dahl, Jarmo Körkkö, Jonna Komulainen‐Ebrahim, Jukka Moilanen, Johanna Uusimaa, Outi Kuismin, Elisa Rahikkala   +14 more
wiley   +1 more source