Results 91 to 100 of about 6,098 (248)
The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician [PDF]
, 2013 A growing number of progressive heredodegenerative conditions mimic the presentation of Huntington's disease (HD). Differentiating among these HD-like syndromes is necessary when a patient with a combination of movement disorders, cognitive decline ...
Bhatia, KP, Martino, D, Stamelou, M
core
Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation [PDF]
, 2017 The allelic disorders rapid-onset dystonia-parkinsonism (RDP), alternating hemiplegia of childhood (AHC), and CAPOS/CAOS syndrome (cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural deafness) are caused by ATP1A3 mutations.1–3
Fawcett, K +7 more
core +2 more sources
Drug and Alcohol Review, Volume 44, Issue 6, Page 1601-1640, September 2025.ABSTRACT Introduction Kava is a plant‐based drug central to many Pacific Island cultures, yet its physiological and psychological effects remain contested and poorly understood. Additionally, the broader social, economic, and policy consequences of kava trade and consumption are unclear.
George Economidis +7 more
wiley +1 more source
, 2003 Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenDystonia is defined as a syndrome of sustained involuntary muscle contractions, frequently causing twisting, repetitive movements and abnormal postures ...
Hilmir Ásgeirsson +1 more
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Biparietal variant of Alzheimer's disease: a rare presentation of a common disease [PDF]
, 2015 Alzheimer's disease (AD) is a clinically heterogeneous disease that may have atypical presentations with focal cortical syndromes and relatively preserved episodic memory.
Marques, IB +3 more
core +1 more source
Case Report: MRI Diagnosis of Wilson's Disease in a 3‐Year‐Old Dalmatian
Veterinary Radiology &Ultrasound, Volume 66, Issue 5, September 2025.ABSTRACT A 3‐year‐old Dalmatian was presented with anorexia, vomiting, and lethargy that progressed to neurological signs with a mixed hepatopathy. MRI identified bilaterally symmetric, ill‐defined hyperintensities in the thalamus, medial and lateral geniculate bodies, and red nuclei on T2‐weighted (T2W) and transverse T2W fluid‐attenuation inversion ...
Natalie Durant +2 more
wiley +1 more source
Skin Signs of Systemic Disease [PDF]
, 1976 The subject of this Mcguire Lecture series, the skin, is a relatively enormous organ vulnerable to an enormous variety of external and internal insults. Its total visibility is both a blessing and a curse.
Scoggins, Robert B.
core +2 more sources
Acute hemichorea as unusual first multiple sclerosis presentation [PDF]
, 2016 Patient 1 was a 39-year-old woman with an unremarkable medical history who developed acute involuntary right arm and leg movements. Neurologic examination revealed moderate dysarthria and subcontinuous, choreic movements in her right limbs, prevailing in
Cavallieri, Francesco +6 more
core +1 more source
Benign hereditary chorea: clinical and neuroimaging features in an Italian family. [PDF]
, 2010 : Benign hereditary chorea is an autosomal domi- nant disorder characterized by early onset nonprogressive chorea, caused by mutations of the thyroid transcription factor-1 (TITF-1) gene.
DE MICHELE, GIUSEPPE +9 more
core +1 more source
Blepharospasm in GNAO1 Syndrome May Benefit From Botulinum Toxins
Movement Disorders Clinical Practice, Volume 12, Issue 11, Page 2007-2009, November 2025.
Eleonora Minacapilli +4 more
wiley +1 more source