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Mostrando 221 - 240 Resultados de 336 Para Buscar '"dandi"', tiempo de consulta: 0.29s Limitar resultados
  1. 221
    “…The infant presented with isolated esophageal atresia (Gross type A), Dandy–Walker malformation, right microphthalmia, left coloboma, overlapping fingers, pleurocentrum in the thoracic vertebrae, reduced anogenital distance, and hearing loss. …”
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    Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature
  2. 222
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    MEK inhibition causes BIM stabilization and increased sensitivity to BCL-2 family member inhibitors in RAS-MAPK-mutated neuroblastoma
  3. 223
    “…Described by Dandy in 1921, the posterior interhemispheric transcallosal approach provides an operative corridor to the pineal region, posterior third ventricle, and upper midbrain. …”
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    Posterior transcallosal intervenous-interforniceal approach to a periaqueductal tumor
  4. 224
    “…The overall clinical phenotype was consistent but not fully diagnostic of craniosynostosis–Dandy–Walker-malformation hydrocephalus syndrome. …”
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    Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives
  5. 225
    “…In some disorders such as Dandy-Walker malformation or Joubert syndrome, the main abnormalities are located within the cerebellum and brainstem. …”
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    Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement
  6. 226
    “…Mega cisterna magna is a part of "Dandy-Walker Complex" and it is characterized by the enlargement of the cisterna magna, morphologically intact vermis and cerebellar hemispheres. …”
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    Manic Episode Associated with Mega Cisterna Magna
  7. 227
    “…We reported a case of PHACE association in a premature infant showing facial, intracranial, and oropharyngeal hemangiomas with evidence of the Dandy-Walker variant and complicated cardiovascular anomalies, including a right-sided aortic arch and an atypical patent ductus arteriosus arising from a tortuous left subclavian artery. …”
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    PHACE association with intracranial, oropharyngeal hemangiomas, and an atypical patent ductus arteriosus arising from the tortuous left subclavian artery in a premature infant
  8. 228
    “…The presence of the nevus prompted brain imaging which showed cortical dysplasia, multiple hamartomas in the temporal lobe, thalamus, and periventricular regions along with cerebellar atrophy and Dandy-Walker variant. To our knowledge, this is the first case in which three different types of brain lesions were found in the same patient.…”
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    First Reported Case of 'Epidermal Nevus Syndrome' with a Triad of Central Nervous System Deformities
  9. 229
    “…Diagnosis is based on modified Dandy criteria after negative clinico-biological and radiological assessment. …”
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    Hypertension intracrânienne idiopathique: à propos d’un cas rare associé à la grossesse
  10. 230
    “…Almost a century ago, Walter Dandy reported dural tenting sutures as an effective way to prevent postoperative EDH. …”
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    Prophylactic use of dural tenting sutures in elective craniotomies in adults—is it necessary? A study protocol for a multicentre, investigator- and participant-blinded randomised, parallel-group, non-inferiority trial
  11. 231
    “…MRI showed characteristics of Dandy–Walker syndrome and ventricular enlargement in the brain. …”
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    Mosaicism trisomy 10 in a 14-month-old child with additional neurological abnormalities: case report and literature review
  12. 232
    “…The MR features of obstructive and communicating hydrocephalus will be discussed, in addition to the manifestations of CSF disorders associated with posterior fossa malformations (Dandy-Walker malformation, Chiari, and Blake’s pouch cyst). …”
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    The value of CSF flow studies in the management of CSF disorders in children: a pictorial review
  13. 233
    por Akins, Paul T., Guppy, Kern H.
    Publicado 2021
    “…Research into the glymphatic system reached an inflection point with steep trajectory in 2012 when it was formally recognized and named, but the historical roots for it are solid and deep, dating back to pioneers such as Cushing, Weed, and Dandy. We provide an overview of key discoveries of the glymphatic system, which promotes bulk flow of fluid and solutes throughout the brain parenchyma. …”
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    Does Impaired Glymphatic Drainage Cause Glymphedema? A Review Tailored to Neurocritical Care and Neurosurgery
  14. 234
    “…This phenotype is similar to those observed in Foxc1 mutant mice and in a human neuroimaging pattern called Dandy Walker malformation. Pdgfc-Pdgfra mutant mice also display ependymal denudation in the fourth ventricle and gene expression changes in cerebellar meninges, which coincide with the first visible signs of cerebellar malformation. …”
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    Severe cerebellar malformations in mutant mice demonstrate a role for PDGF-C/PDGFRα signalling in cerebellar development
  15. 235
    “…Tetrasomy 9p is a rare syndrome characterized by fetal growth restriction, Dandy-Walker malformation, cardiac anomalies, and facial abnormalities and is discovered by ultrasound during the prenatal examination. …”
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    Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing
  16. 236
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    P366: ARE MINIMAL RESIDUAL DISEASE MEASUREMENTS AFTER CONSOLIDATION THERAPY USEFUL IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA?
  17. 237
    por Dandy, Walter E.
    Publicado 1915
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    EXTIRPATION OF THE PINEAL BODY
  18. 238
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    Intramural hematoma of the esophagus mimicking hemorrhaging esophageal cancer
  19. 239
    “…Detected anomalies were as follow: 3 (16.6%) fetuses each had the Dandy-Walker variant and Arnold-Chiari II (with myelomeningocele). …”
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    Fetal Central Nervous System Anomalies Detected by Magnetic Resonance Imaging: A Two-Year Experience
  20. 240
    “…Of these 17 patients, eight patients (47.1%) had hydrocephaly, one patient (5.8%) with Dandy Walker syndrome. Micrognathia, macroglossia, restriction in neck movements were recorded as the reasons in six cases each. …”
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    Airway management for occipital encephalocele in neonatal patients: A review of 17 cases
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