Robson CD - Search Results

1

Cockayne syndrome: the developing phenotype.

Tan WH, Baris H, Robson CD, Kimonis VE. Tan WH, et al. Among authors: robson cd. Am J Med Genet A. 2005 Jun 1;135(2):214-6. doi: 10.1002/ajmg.a.30731. Am J Med Genet A. 2005. PMID: 15887300 Free article.

2

Intracranial anomalies detected by imaging studies in 30 patients with Apert syndrome.

Quintero-Rivera F, Robson CD, Reiss RE, Levine D, Benson CB, Mulliken JB, Kimonis VE. Quintero-Rivera F, et al. Among authors: robson cd. Am J Med Genet A. 2006 Jun 15;140(12):1337-8. doi: 10.1002/ajmg.a.31277. Am J Med Genet A. 2006. PMID: 16691624 Free article. No abstract available.

3

Apert syndrome: what prenatal radiographic findings should prompt its consideration?

Quintero-Rivera F, Robson CD, Reiss RE, Levine D, Benson C, Mulliken JB, Kimonis VE. Quintero-Rivera F, et al. Among authors: robson cd. Prenat Diagn. 2006 Oct;26(10):966-72. doi: 10.1002/pd.1539. Prenat Diagn. 2006. PMID: 16906598 Free article.

4

The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.

Tan WH, Baris HN, Burrows PE, Robson CD, Alomari AI, Mulliken JB, Fishman SJ, Irons MB. Tan WH, et al. Among authors: robson cd. J Med Genet. 2007 Sep;44(9):594-602. doi: 10.1136/jmg.2007.048934. Epub 2007 May 25. J Med Genet. 2007. PMID: 17526801 Free PMC article.

5

Encephalocraniocutaneous lipomatosis accompanied by the formation of bone cysts: Harboring clues to pathogenesis?

Moog U, Roelens F, Mortier GR, Sijstermans H, Kelly M, Cox GF, Robson CD, Kimonis VE. Moog U, et al. Among authors: robson cd. Am J Med Genet A. 2007 Dec 15;143A(24):2973-80. doi: 10.1002/ajmg.a.31957. Am J Med Genet A. 2007. PMID: 18000896 Free article.

6

Neuroimaging in Kabuki syndrome and another KMT2D-related disorder.

Stadelmaier RT, Kenna MA, Barrett D, Mullen TE, Bodamer O, Agrawal PB, Robson CD, Wojcik MH. Stadelmaier RT, et al. Among authors: robson cd. Am J Med Genet A. 2021 Dec;185(12):3770-3783. doi: 10.1002/ajmg.a.62450. Epub 2021 Aug 9. Am J Med Genet A. 2021. PMID: 34369642 Free PMC article.

7

Radiologic-Pathologic Conference of Children's Hospital Boston: scalp mass in a child following treatment for craniopharyngioma.

Robson CD, Barnes PD, Taylor GA, Rodriguez ML. Robson CD, et al. Pediatr Radiol. 1996;26(3):236-8. doi: 10.1007/BF01405308. Pediatr Radiol. 1996. PMID: 8599018

8

Imaging of pediatric temporal bone abnormalities.

Robson CD, Robertson RL, Barnes PD. Robson CD, et al. Neuroimaging Clin N Am. 1999 Feb;9(1):133-55. Neuroimaging Clin N Am. 1999. PMID: 9974503 Review.

9

Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing?

Kenna MA, Rehm HL, Robson CD, Frangulov A, McCallum J, Yaeger D, Krantz ID. Kenna MA, et al. Among authors: robson cd. Am J Med Genet A. 2007 Jul 15;143A(14):1560-6. doi: 10.1002/ajmg.a.31706. Am J Med Genet A. 2007. PMID: 17455295

10

Acute hydrocephalus secondary to obstruction of the foramen of monro and cerebral aqueduct caused by a choroid plexus cyst in the lateral ventricle. Case report.

Nahed BV, Darbar A, Doiron R, Saad A, Robson CD, Smith ER. Nahed BV, et al. Among authors: robson cd. J Neurosurg. 2007 Sep;107(3 Suppl):236-9. doi: 10.3171/PED-07/09/236. J Neurosurg. 2007. PMID: 17918533

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