Results 61 to 70 of about 188,196 (282)
Effective resource allocation for architectural heritage conservation requires reliable and up-to-date data to support proper decision-making. This paper proposes a novel methodology for the integration of reviews continuously generated by users with ...
Marco D’Orazio +3 more
semanticscholar +1 more source
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando +13 more
wiley +1 more source
Scoliosis Surgery in a Patient With Advanced Friedreich's Ataxia—It Is Not Too Late
ABSTRACT Friedreich's ataxia is a multisystem disorder with scoliosis being the most common non‐neurological manifestation. While scoliosis surgery is typically performed in adolescent, ambulatory patients, few data exist on surgical outcomes in patients with advanced disease.
Kathrin Reetz +20 more
wiley +1 more source
Language Revitalization: The case of Judeo-Spanish varieties in Macedonia [PDF]
Judeo-Spanish is a secondary dialect of the Spanish language having evolved from the ancient standard Spanish in the course of its expansion southwards. Although the language enjoys a heritage and presence in the Balkans of over five centuries, it is now
Zarghooni-Hoffmann, Esther
core
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun +95 more
wiley +1 more source
The Descriptive Challenges of Fiber Art [PDF]
published or submitted for ...
Lunin, Lois F.
core
RAB39B Related Parkinsonism in an Italian Family: A Unique Use of Advanced Therapies
ABSTRACT Parkinson's disease (PD) is a neurodegenerative disorder that may sometimes be caused by deleterious genetic variants. Among them, RAB39B polymorphisms are known as rare causes of early‐onset PD associated with intellectual disability (Waisman's syndrome).
Caterina Del Regno +13 more
wiley +1 more source
The programming language PHP is a mixture of different programming languages. Mainly, it uses the syntax that most of the programmers knows of the programming language C, but is very different from this last one, since PHP is an interpreted programming ...
Nadia Villarejo Sánchez
doaj
Special Libraries, January 1953 [PDF]
Volume 44, Issue 1https://scholarworks.sjsu.edu/sla_sl_1953/1000/thumbnail ...
Special Libraries Association
core +4 more sources
Nationwide Survey of Atopic Myelitis and Plexin D1‐Immunoglobulin G‐Related Pain
ABSTRACT Objective To elucidate the features of plexin D1‐immunoglobulin (Ig)G‐associated neuropathic pain and its relationship to atopic myelitis (AM) in a nationwide Japanese survey. Methods A preliminary survey questionnaire was sent to 1574 selected departments (neurology and pediatrics/pediatric neurology) to explore the numbers of AM and plexin ...
Jun‐ichi Kira +10 more
wiley +1 more source

