Results 111 to 120 of about 55,874 (244)
, 2021 La séance du 11 mai se déroulera sur Zoom à 18h30. Sujet : Ovale Seminaire Le Bruit Heure : 11 mai 2021 18:30 PM Paris Participer à la réunion Zoom https://zoom.us/j/98917104220?pwd=VmZlb0llNFhyRU1UVHR3K0V0L1JUUT09 ID de réunion : 989 1710 4220 Code
ovale
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Infantile Epileptic Spasms Syndrome Complicating Mosaic Down‐Turner Syndrome: A Case Report
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Severe baseline developmental delays in complex genetic syndromes like Down‐Turner mosaicism can completely mask the psychomotor regression of Infantile Epileptic Spasms Syndrome (IESS). Clinicians must maintain a high index of suspicion and prioritize early video‐EEG screening for any abnormal paroxysmal movements.
Mohammad Shahrori +4 more
wiley +1 more source
Percutaneous closure of the patent foramen ovale
, 2007 A patent foramen ovale (PFO) is a common finding present in 25% of the population. A relationship between PFO and several clinical conditions such as stroke, migraine, platypnea-orthodeoxia syndrome, neurological decompression illness in divers, high ...
Meier, B, Surmely, J-F
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Patent foramen ovale increases stroke risk in older people
, 2018 Patent foramen ovale (PFO) is prevalent among young patients with cryptogenic stroke, and PFO closure reduces the risk of recurrent stroke in these individuals.
Saver, J. L. +3 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT The colon single stripe sign (CSSS) is associated with ischemic‐pattern colonic injury. We report a 69‐year‐old woman with norovirus infection, hematochezia, recurrent left‐sided colitis, and chronic NSAID use found to have CSSS on colonoscopy, suggesting a multifactorial “two‐hit” mechanism involving NSAID‐related mucosal vulnerability and ...
Sushrut Ingawale +7 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Patau syndrome (trisomy 13) is a life‐limiting chromosomal disorder with multiple congenital anomalies. We report a term male neonate with bilateral cleft lip and palate, aplasia cutis congenita, postaxial polydactyly, hypotonia, congenital heart disease, and presumed neonatal sepsis.
Sayed Hussain Amiri +4 more
wiley +1 more source
, 2017 Ce carnet est destiné à rendre compte du travail de recherche collectif et individuel des doctorants anglicistes de Paris IV. Il s'agit d'un cahier partagé par les membres du laboratoire junior rattaché à VALE (ED4 EA4085).
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Importância do Foramen Ovale Permeável, no Adulto [PDF]
, 2018 O Foramen Ovale Permeável é a cardiopatia congénita mais frequente, estando presente em aproximadamente 25% da população adulta em todo o mundo. Relativamente à influência do sexo e da idade no Foramen Ovale Permeável, conclui-se que a sua frequência e ...
Mourão, Natacha Batista
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An atypical position of the foramen ovale.
Folia morphologica, 2006 Visual inspection of a dry adult human skull revealed absence of a typical foramen ovale on the left side of the cranial base. The region of the foramen ovale was covered by an osseous lamina, which was continuous with the lateral pterygoid plate and thus formed a wall of an apparent canal, which opened on the lateral side of the pterygoid process ...
Skrzat, Janusz +3 more
openaire +2 more sources