Results 201 to 210 of about 653,899 (348)
Comparison of warfarin and aspirin for symptomatic intracranial arterial stenosis.
M. Chimowitz +12 more
semanticscholar +1 more source
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates +6 more
wiley +1 more source
Intracranial Dural Arteriovenous Fistulae
M. Reynolds, G. Lanzino, G. Zipfel
semanticscholar +1 more source
ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston +35 more
wiley +1 more source
Occipital Extracranial Dermoid Cyst in a Neonate With Cardiofaciocutaneous Syndrome Type 4 (CFC4): A Case Report. [PDF]
Alkallabi M +4 more
europepmc +1 more source
Prevalence and risk of rupture of intracranial aneurysms: a systematic review.
G. Rinkel, M. Djibuti, A. Algra, J. Gijn
semanticscholar +1 more source
ABSTRACT Homozygous achondroplasia is widely considered perinatal lethal by the medical community. In this case series, we report two children from a single family with longer‐term survival. One child lived for 17 months and the other was 60 months at the time of publication.
Hannah Singerline +3 more
wiley +1 more source
Effect of intravenous alteplase before endovascular therapy for atherothrombotic stroke-related large vessel occlusion: subanalysis of the RESCUE AT-LVO registry. [PDF]
Hayashi H +27 more
europepmc +1 more source

