Blaser S - Search Results

1

Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndrome.

Gillis J, Burashnikov E, Antzelevitch C, Blaser S, Gross G, Turner L, Babul-Hirji R, Chitayat D. Gillis J, et al. Among authors: blaser s. Am J Med Genet A. 2012 Jan;158A(1):182-7. doi: 10.1002/ajmg.a.34355. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22106044 Free PMC article.

2

Cavum veli interpositi: prenatal diagnosis and postnatal outcome.

Shah PS, Blaser S, Toi A, Fong K, Glanc P, Babul-Hirji R, Rutka J, Chitayat D. Shah PS, et al. Among authors: blaser s. Prenat Diagn. 2005 Jul;25(7):539-42. doi: 10.1002/pd.1114. Prenat Diagn. 2005. PMID: 16034837

3

Prenatal US and MR imaging findings of lissencephaly: review of fetal cerebral sulcal development.

Ghai S, Fong KW, Toi A, Chitayat D, Pantazi S, Blaser S. Ghai S, et al. Among authors: blaser s. Radiographics. 2006 Mar-Apr;26(2):389-405. doi: 10.1148/rg.262055059. Radiographics. 2006. PMID: 16549605 Review.

4

Prenatal detection of microtia by MRI in a fetus with trisomy 22.

Milic A, Blaser S, Robinson A, Viero S, Halliday W, Winsor E, Toi A, Thomas M, Chitayat D. Milic A, et al. Among authors: blaser s. Pediatr Radiol. 2006 Jul;36(7):706-10. doi: 10.1007/s00247-006-0155-9. Epub 2006 Apr 25. Pediatr Radiol. 2006. PMID: 16770674

5

Molar tooth sign in fetal brain magnetic resonance imaging leading to the prenatal diagnosis of Joubert syndrome and related disorders.

Fluss J, Blaser S, Chitayat D, Akoury H, Glanc P, Skidmore M, Raybaud C. Fluss J, et al. Among authors: blaser s. J Child Neurol. 2006 Apr;21(4):320-4. doi: 10.1177/08830738060210041001. J Child Neurol. 2006. PMID: 16900929

6

Duodenal and biliary atresia associated with facial, thyroid and auditory apparatus abnormalities: a new mandibulofacial dysostosis syndrome?

Maegawa GHB, Chitayat D, Blaser S, Whyte H, Thomas M, Kim P, Kim J, Taylor G, McNamara PJ. Maegawa GHB, et al. Among authors: blaser s. Clin Dysmorphol. 2006 Oct;15(4):191-196. doi: 10.1097/01.mcd.0000198932.09330.33. Clin Dysmorphol. 2006. PMID: 16957470 Review.

7

The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance.

Chitayat D, Sroka H, Keating S, Colby RS, Ryan G, Toi A, Blaser S, Viero S, Devisme L, Boute-Bénéjean O, Manouvrier-Hanu S, Mortier G, Loeys B, Rauch A, Bitoun P. Chitayat D, et al. Among authors: blaser s. Am J Med Genet A. 2007 Jun 15;143A(12):1268-81. doi: 10.1002/ajmg.a.31788. Am J Med Genet A. 2007. PMID: 17506106

8

Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings.

Chitayat D, Shannon P, Keating S, Toi A, Blaser S, Friedberg T, Superti-Furga A, Chong K, Unger S. Chitayat D, et al. Among authors: blaser s. Am J Med Genet A. 2007 Dec 15;143A(24):3280-5. doi: 10.1002/ajmg.a.32022. Am J Med Genet A. 2007. PMID: 18000911

9

MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlation.

Robinson AJ, Blaser S, Toi A, Chitayat D, Pantazi S, Keating S, Viero S, Ryan G. Robinson AJ, et al. Among authors: blaser s. Pediatr Radiol. 2008 Sep;38(9):971-81. doi: 10.1007/s00247-008-0929-3. Epub 2008 Jul 17. Pediatr Radiol. 2008. PMID: 18633608

10

Abnormalities of the foetal cerebral cortex.

Toi A, Chitayat D, Blaser S. Toi A, et al. Among authors: blaser s. Prenat Diagn. 2009 Apr;29(4):355-71. doi: 10.1002/pd.2211. Prenat Diagn. 2009. PMID: 19235759 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

392 results

Search Page