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  1. 261
    “…In the context of early second-trimester screening, upward rotation of the cerebellar vermis per se is usually compatible with a more favorable outcome than Dandy-Walker malformation and profound vermian hypoplasia. …”
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    Delayed fenestration of Blake’s pouch with or without vermian hypoplasia: fetal MRI at 3 tesla versus 1.5 tesla
  2. 262
    “…Syndrome diagnosis is often missed at prenatal ultrasound and fetal autopsy METHODS: We performed autopsies and DHCR7 gene analyses in eight fetuses suspected of having SLOS and measured cholesterol values in long‐term formalin‐fixed tissues of an additional museum exhibit RESULTS: Five of the nine fetuses presented classical features of SLOS, including four cases with atrial/atrioventricular septal defects and renal anomalies, and one with additional bilateral renal agenesis and a Dandy‐Walker cyst. These cases allowed for diagnosis at autopsy and subsequent SLOS diagnosis in two siblings. …”
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    Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern
  3. 263
    “…CASE DESCRIPTION: A 24-year-old woman presented with a history of ventriculostomy and ventriculoperitoneal shunt (VPS) secondary to hydrocephalus concomitant with Dandy-Walker syndrome. She has had undulant headache and vision loss episodes in both eyes for 15 days. …”
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    Shunt Valve Rupture in Ventriculoperitoneal Shunt Failure
  4. 264
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    Anticipating environmental losses: Effects on place attachment and intentions to move
  5. 265
    por Koo, H., Chi, J. G.
    Publicado 1991
    “…Twenty-five cases associated with congenital malformation of the CNS consisted of 10 cases of holotelencephaly, 5 cases of stenosis of the Sylvian aqueduct, 4 cases of agenesis of the corpus callosum, and 3 cases each of Dandy-Walker malformation and Arnold-Chiari malformation. …”
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    Congenital hydrocephalus--analysis of 49 cases.
  6. 266
    por Wang, Lei, Dandy, David S.
    Publicado 2017
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    High‐Throughput Inertial Focusing of Micrometer‐ and Sub‐Micrometer‐Sized Particles Separation
  7. 267
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    Electrochemical Capillary Driven Immunoassay for Detection of SARS-CoV-2
  8. 268
    “…CASE DESCRIPTION: Newborn at 38 weeks of gestation by cesarean section, with congenital hydrocephalus due to Dandy–Walker malformation that required right Frazier VPS placement. …”
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    Intracranial migration of a ventriculoperitoneal shunt: A case report and literature review
  9. 269
    “…MRI revealed no space-occupying lesions, and the patient was diagnosed with IIH based on the modified Dandy criteria. MR venography revealed stenosis in the right and hypoplastic left TS. …”
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    The Case of a Patient with Idiopathic Intracranial Hypertension Who Required Additional Stenting for Stent-Adjacent Stenosis
  10. 270
    “…Sixty-three fetuses had fetal CNS abnormalities of acrania, anencephaly, encephalocele, Dandy-Walker malformation, hydrocephalus, and meningocele. …”
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    The Relationship Between Fetal Central Nervous System Malformations and Modified Myocardial Performance Index
  11. 271
    “…USP9X was recently linked with syndromic cognitive impairment that includes hearing loss, dental defects, ventriculomegaly, Dandy–Walker malformation, skeletal anomalies (hip dysplasia), and other features showing a significant overlap with FOXC1-ARS. …”
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    Alternative Genetic Diagnoses in Axenfeld–Rieger Syndrome Spectrum
  12. 272
    “…Analysis was done for 50/106 patients who fulfilled modified Dandy's criteria and had optic disc edema and a minimal follow-up period of two years. …”
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    Clinical profile, evaluation, management and visual outcome of idiopathic intracranial hypertension in a neuro-ophthalmology clinic of a tertiary referral ophthalmic center in India
  13. 273
    “…Eighteen cases (29%) with spinal dysraphism, 15 cases (24%) with acqueductal stenosis, 9 (14.5%) post meningitis, 6 (9.7%) post haemorrhagic, 6 (9.7%) with structural Central Nervous System (CNS) anomalies (holoprosencephaly 2, hemispheric cysts 2, brain dysgenesis 1, and vascular anomaly 1), 3 (4.9%) congenital idiopathic, 2 (3.2%) Dandy-Walker malformation, 2 (3.2%) toxoplasmosis and one case (1.6%) achondroplasia. …”
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    INFANTILE HYDROCEPHALUS IN SOUTHERN SAUDI ARABIA
  14. 274
    “…Postnatal MRI was consistent with Dandy-Walker variant showing hypogenesis of the inferior cerebellar vermis. …”
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    Prenatal Identification and Molecular Characterization of Two Simultaneous De Novo Interstitial Duplications of Chromosomal Regions 7p22.1p21.1 and 15q24.1
  15. 275
    “…The patients were evaluated and diagnosed based on clinical judgement as well as using the modified Dandy criteria. RESULTS: All six patients were female and all except one were obese. …”
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    Case series of six patients diagnosed and managed for idiopathic intracranial hypertension at a tertiary institution eye centre
  16. 276
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    Giant stone in a urinary bladder diverticulum in a 69-year-old male: a case report
  17. 277
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    Percutaneous nephrolithotomy for management neglected encrusted ureteral stent in a transplanted kidney: a case report
  18. 278
    “…A 4-month-old girl with a Dandy-Walker malformation underwent a ventriculoperitoneal shunt procedure. …”
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    Slit ventricle syndrome and early-onset secondary craniosynostosis in an infant
  19. 279
    “…BACKGROUND: We report a case of a neonate with proximal spinal muscular atrophy (SMA) type 1 (also known as Werdnig-Hoffmann disease or severe infantile acute SMA) associated with a Blake's pouch cyst; a malformation that is currently classified within the spectrum of Dandy-Walker complex. The association of the two conditions has not been previously reported in the English literature. …”
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    Blake's pouch cyst and Werdnig-Hoffmann disease: Report of a new association and review of the literature
  20. 280
    “…DIAGNOSES: The prenatal phenotype of case 1 included sonographic markers such as enlarged nuchal translucency (NT), absent nasal bone, short femur and humerus length, and several structural malformations involving Dandy–Walker malformation and congenital heart defects. …”
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    Uniparental disomy and prenatal phenotype: Two case reports and review
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