Results 141 to 150 of about 196,484 (310)
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
Overseas Relief, Europe: Germany (ASF AR 1, Box 1, Folder 22)
, 1943 Digital ImageDigital finding aid ...
Central Sephardic Jewish Community of America
core
Cultural Diplomacy and Informal Artistic Relations in East Central Europe in the 20th Century
This Special Issue brings together a diverse group of scholars to engage in critical dialogue on the history and socio-political foundations of international traveling art exhibitions and cultural exchange.
core +1 more source
Multiple Sclerosis Relapse Activity After Ozanimod Discontinuation in DAYBREAK Trial Participants
Annals of Clinical and Translational Neurology, EarlyView.Multiple Sclerosis Relapse Activity After Ozanimod Discontinuation in DAYBREAK Trial Participants. ABSTRACT Objective Return of disease activity is expected when patients discontinue disease‐modifying therapy (DMT) for multiple sclerosis (MS). Some MS DMTs are associated with higher‐than‐expected disease activity (rebound) after discontinuation.
Ralf Gold +12 more
wiley +1 more source
Overseas Relief, Europe: Greece (ASF AR 1, Box 1, Folder 23)
, 1944 Digital ImageDigital finding aid ...
Central Sephardic Jewish Community of America
core
SPG4 and Dementia: Expanding the Clinical Spectrum
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Overseas Relief, Europe: France (ASF AR 1, Box 1, Folder 21)
, 1945 Digital ImageDigital finding aid ...
Central Sephardic Jewish Community of America
core
On the Margins of European History
, 2020 Jitka Malečková The idea of European history, which is closely tied up with the notoriously elusive concept of Europe, has meant and continues to mean different things to different groups and individuals, including historians, in different times and ...
EuropeDebate
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Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source
Diacronie. Studi di Storia Contemporanea, 2018 Although far from the centres of conflict on the Continent, interwar Ireland was also exposed to the influence of extreme left and right-wing political movements. Overall, most Irish nationalists adopted an uncompromisingly anti-Communist stance and used
Lili Zách has received her Masters Degrees in English (with specialization in Irish Studies) and History at the University of Szeged, Hungary, in 2006. She completed a PhD at the National University of Ireland, Galway, focusing on Irish perceptions of the small successor states of Austria-Hungary, 1914-1945. Her primary research interest lies in the field of Irish and Central European history in a transnational framework, with special attention to Irish links with Continental Europe in the first half of the twentieth century.
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