Results 71 to 80 of about 24,265 (289)
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane +43 more
wiley +1 more source
Conceptions of truth in relation to the sciences vary extensively along two dimensions. The first concerns the applicability of the notion of truth to scientific knowledge, resulting in a number of contentions regarding the relevance or importance of ...
Chakravartty, Anjan
core +1 more source
The Ontological Foundation of Allameh Tabatabaei’s View on
In Islamic philosophy various interpretations are offered with respect to the concept “Nafs al-Amr”. These have resulted from the way different philosophers have tried to resolve the difficulties concerning the correspondence theory of truth in ...
jafar shanazari, ahmad Sadeghi
doaj
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
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
Metasemantics, moderate inflationism, and correspondence truth [PDF]
An object-based correspondence theory of truth holds that a truth-bearer is true whenever its truth conditions are met by objects and their properties.
Moore, Graham Seth
core
In Islamic philosophy various interpretations are offered with respect to the concept “Nafs al-Amr”. These have resulted from the way different philosophers have tried to resolve the difficulties concerning the correspondence theory of truth in ...
Dr jafar shanazari, Ahmad Sadeghi
doaj
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
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
Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach +23 more
wiley +1 more source
ABSTRACT Introduction Glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs) have demonstrated significant weight‐reducing effects and may offer benefits in idiopathic intracranial hypertension (IIH); however, recent concerns about the risk of non‐arteritic anterior ischemic optic neuropathy (NAION) have emerged.
Faisal A. Al‐Harbi +9 more
wiley +1 more source
The Concept of ‘Truth’ in Legal Science: A Theoretical Exploration
The author explores the concept of “truth” in jurisprudence, positioning it both as the ultimate goal of legal research and as an autonomous entity with independent value due to its ability to reflect objective reality in scientific knowledge.
Pavel L. Likhter
doaj +1 more source

