Pugash D - Search Results

1

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Lehman AM, McFadden D, Pugash D, Sangha K, Gibson WT, Patel MS. Lehman AM, et al. Among authors: pugash d. Am J Med Genet A. 2008 May 15;146A(10):1299-306. doi: 10.1002/ajmg.a.32277. Am J Med Genet A. 2008. PMID: 18398855

2

Fetal progeria: prenatal sonographic findings in petty syndrome.

Pugash D, Schrader KA, Dunham CP, Popescu OE, Sargent MA, Lehman AM, Yong SL, Clarke LA. Pugash D, et al. J Ultrasound Med. 2013 May;32(5):881-3. doi: 10.7863/ultra.32.5.881. J Ultrasound Med. 2013. PMID: 23620331 No abstract available.

3

Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia.

Pugash D, Lehman AM, Langlois S. Pugash D, et al. Ultrasound Obstet Gynecol. 2014 Sep;44(3):365-8. doi: 10.1002/uog.13359. Ultrasound Obstet Gynecol. 2014. PMID: 24616001 Free article.

4

Additional post-natal diagnoses following antenatal diagnosis of isolated cleft lip +/− palate.

Burnell L, Verchere C, Pugash D, Loock C, Robertson S, Lehman A. Burnell L, et al. Among authors: pugash d. Arch Dis Child Fetal Neonatal Ed. 2014 Jul;99(4):F286-90. doi: 10.1136/archdischild-2013-305390. Epub 2014 Mar 13. Arch Dis Child Fetal Neonatal Ed. 2014. PMID: 24625434

5

Prenatal and postnatal findings in serpentine fibula polycystic kidney syndrome and a review of the NOTCH2 spectrum disorders.

Martin BM, Ivanova MH, Sarukhanov A, Kim A, Power P, Pugash D, Popescu OE, Lachman RS, Krakow D, Patel MS. Martin BM, et al. Among authors: pugash d. Am J Med Genet A. 2014 Oct;164A(10):2490-5. doi: 10.1002/ajmg.a.36656. Epub 2014 Jul 3. Am J Med Genet A. 2014. PMID: 24995648

6

Expanding the FANCO/RAD51C associated phenotype: Cleft lip and palate and lobar holoprosencephaly, two rare findings in Fanconi anemia.

Jacquinet A, Brown L, Sawkins J, Liu P, Pugash D, Van Allen MI, Patel MS. Jacquinet A, et al. Among authors: pugash d. Eur J Med Genet. 2018 May;61(5):257-261. doi: 10.1016/j.ejmg.2017.12.011. Epub 2017 Dec 24. Eur J Med Genet. 2018. PMID: 29278735

7

Prenatal ultrasound and fetal MRI: the comparative value of each modality in prenatal diagnosis.

Pugash D, Brugger PC, Bettelheim D, Prayer D. Pugash D, et al. Eur J Radiol. 2008 Nov;68(2):214-26. doi: 10.1016/j.ejrad.2008.06.031. Epub 2008 Sep 14. Eur J Radiol. 2008. PMID: 18790583 Review.

8

Pre- and postnatal findings in a boy with duplication of the bladder and intestine: report and review.

Alfadhel M, Pugash D, Robinson AJ, Murphy JJ, Senger C, Afshar K, Armstrong L. Alfadhel M, et al. Among authors: pugash d. Am J Med Genet A. 2009 Dec;149A(12):2795-802. doi: 10.1002/ajmg.a.33091. Am J Med Genet A. 2009. PMID: 19921644 Review.

9

Beckwith-Wiedemann syndrome in sibs discordant for IC2 methylation.

Niederhoffer KY, Peñaherrera M, Pugash D, Rupps R, Arbour L, Tessier F, Choufani S, Zhao C, Manokhina I, Shuman C, Robinson WP, Weksberg R, Boerkoel CF. Niederhoffer KY, et al. Among authors: pugash d. Am J Med Genet A. 2012 Jul;158A(7):1662-9. doi: 10.1002/ajmg.a.35377. Epub 2012 May 21. Am J Med Genet A. 2012. PMID: 22615066

10

Sonographic 'molar tooth' sign in the diagnosis of Joubert syndrome.

Pugash D, Oh T, Godwin K, Robinson AJ, Byrne A, Van Allen MI, Osiovich H. Pugash D, et al. Ultrasound Obstet Gynecol. 2011 Nov;38(5):598-602. doi: 10.1002/uog.8979. Ultrasound Obstet Gynecol. 2011. PMID: 21370303 Free article.

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