Results 41 to 50 of about 608,971 (305)
ABSTRACT Background Central nervous system (CNS) neuroblastoma, FOXR2‐activated, is a recently recognized entity in the WHO CNS5 classification, defined by activation of the FOXR2 transcription factor and unique histopathological features. This review synthesizes available literature and pooled clinical data, providing insight into demographics ...
Sudarshawn Damodharan +1 more
wiley +1 more source
Locations: B (ASF AR 1, Box 1, Folder 43) [PDF]
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Central Sephardic Jewish Community of America
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ABSTRACT Background Cerebellar ataxia after pediatric brain tumor treatment can cause persistent gait, balance, and speech impairment, yet no established rehabilitation strategy exists. Somato‐cognitive coordination therapy (SCCT) is a virtual reality–guided intervention designed to promote sensorimotor integration through visually constrained reaching
Masanobu Takeuchi +10 more
wiley +1 more source
Immigration: Inactive (ASF AR 1, Box 1, Folder 7) [PDF]
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Central Sephardic Jewish Community of America
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Attributing daily ocean temperatures to anthropogenic climate change
Ocean temperatures are rising and hit record levels around the world in 2023. While trends are clear and likely strongly connected to human-caused climate change, the oceans also exhibit variability on the daily level, leading to local extremes such as ...
Joseph Giguere +2 more
doaj +1 more source
Introduction: Prosthetic valve endocarditis (PVE) is a known complication of prosthetic valve implantation (PVI). Native valve endocarditis (INVE) without concurrent PVE, or isolated native valve endocarditis (INVE), after PVI is largely unheard of in ...
Sujoy Khasnavis +6 more
doaj +1 more source
Ten amber inclusions of male Ripidiinae (Coleoptera: Ripiphoridae) are reported from Early Miocene deposits of the Dominican Republic and compared with extant species of Neorrhipidius Viana, 1958 from Argentina and Paraguay and Quasipirhidius Zaragoza ...
Jan BATELKA +3 more
doaj +1 more source
ABSTRACT Background Type 1 plasminogen deficiency (PLGD‐1) is an ultra‐rare autosomal recessive disorder caused by variants in the PLG gene and affects approximately 1.6 individuals per million. The condition is characterized by decreased plasminogen levels and impaired function, resulting in fibrin‐rich lesions on mucous membranes throughout the body.
Charles Nakar +7 more
wiley +1 more source
Locations: E-F (ASF AR 1, Box 1, Folder 50) [PDF]
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Central Sephardic Jewish Community of America
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