Results 71 to 80 of about 5,725 (256)

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

Surgical rarities: case report of appendicular diverticulitis and literature review. [PDF]

open access: yesJ Surg Case Rep, 2022
Bonomo LD   +8 more
europepmc   +1 more source

Homologació de rareses ornitològiques a Balears. Informe de 2011 [PDF]

open access: yes
Homologació de rareses ornitològiques a Balears. Informe de 2011. 21è informe anual que presenta el comitè de rareses Ornitològiques de Balears. S’han homologat 27 registres, corresponents a les següents espècies, ànnera canyella Tadorna ferruginea ...
García-Febrero, Òscar   +5 more
core  

Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein   +13 more
wiley   +1 more source

Whole‐Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize whole‐body intramuscular fat distribution pattern in patients with sarcoglycanopathies and explore correlations with disease severity, duration and age at onset. Methods Retrospective, cross‐sectional, multicentric study enrolling patients with variants in one of the four sarcoglycan genes who underwent whole‐body ...
Laura Costa‐Comellas   +39 more
wiley   +1 more source

Numerical analysis of distribution patterns in the British and European floras [PDF]

open access: yes, 2007
Imperial Users ...
Finnie, Thomas James Ronald   +1 more
core  

Spinal Cord Infarction Versus Idiopathic Transverse Myelitis: Clinical, Radiological, and Functional Insights From a Retrospective Cohort Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Spinal cord infarction (SCI) is a rare but devastating myelopathy, characterized by a high disability rate and an unfavorable prognosis. It has often been underdiagnosed and misdiagnosed as idiopathic transverse myelitis (ITM). This study aimed to describe the clinical features, radiological biomarkers, treatments, and functional ...
Zeqiang Ji   +13 more
wiley   +1 more source

Homologació de rareses ornitològiques a Mallorca i Formentera. Informe de 1994 [PDF]

open access: yes
Quart informe anual del Comitè d'Homologació de Rareses a Mallorca i Formentera. Se presenten 38 registres, la majoria de 1994. Se n'accepten 31 (81%). Entre ells destaquen els primers registres segurs d'ànnera glacial (Clangula hyemalis), rasclet petit (
López-Jurado, Carlos
core  

Bosnia and Hercegovina [PDF]

open access: yes, 2001
Bosnia-Hercegovina declared sovereignty and seceded from the residue of the Socialist Federal Republic of Yugoslavia (SFRJ) in October 1991, following similar action, first by Slovenia, then by Croatia and after a plebiscite, boycotted by many ethnic ...
Clarke, Richard
core  

Remote Assessment of Ataxia Severity in SCA3 Across Multiple Centers and Time Points

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinocerebellar ataxia type 3 (SCA3) is a genetically defined ataxia. The Scale for Assessment and Rating of Ataxia (SARA) is a clinician‐reported outcome that measures ataxia severity at a single time point. In its standard application, SARA fails to capture short‐term fluctuations, limiting its sensitivity in trials.
Marcus Grobe‐Einsler   +20 more
wiley   +1 more source

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