Saal HM - Search Results

1

The Use of Magnetic Resonance Imaging Screening for Optic Pathway Gliomas in Children with Neurofibromatosis Type 1.

Prada CE, Hufnagel RB, Hummel TR, Lovell AM, Hopkin RJ, Saal HM, Schorry EK. Prada CE, et al. Among authors: saal hm. J Pediatr. 2015 Oct;167(4):851-856.e1. doi: 10.1016/j.jpeds.2015.07.001. Epub 2015 Jul 29. J Pediatr. 2015. PMID: 26233602 Free PMC article.

2

Pediatric plexiform neurofibromas: impact on morbidity and mortality in neurofibromatosis type 1.

Prada CE, Rangwala FA, Martin LJ, Lovell AM, Saal HM, Schorry EK, Hopkin RJ. Prada CE, et al. Among authors: saal hm. J Pediatr. 2012 Mar;160(3):461-7. doi: 10.1016/j.jpeds.2011.08.051. Epub 2011 Oct 11. J Pediatr. 2012. PMID: 21996156

3

Thoracic tumors in children with neurofibromatosis-1.

Schorry EK, Crawford AH, Egelhoff JC, Lovell AM, Saal HM. Schorry EK, et al. Among authors: saal hm. Am J Med Genet. 1997 Sep 19;74(5):533-7. doi: 10.1002/(sici)1096-8628(19970919)74:5<533::aid-ajmg16>3.0.co;2-d. Am J Med Genet. 1997. PMID: 9342207

4

Social and emotional problems in children with neurofibromatosis type 1: evidence and proposed interventions.

Johnson NS, Saal HM, Lovell AM, Schorry EK. Johnson NS, et al. Among authors: saal hm. J Pediatr. 1999 Jun;134(6):767-72. doi: 10.1016/s0022-3476(99)70296-9. J Pediatr. 1999. PMID: 10356149

5

Evaluation of growth in patients with isolated cleft lip and/or cleft palate.

Zarate YA, Martin LJ, Hopkin RJ, Bender PL, Zhang X, Saal HM. Zarate YA, et al. Among authors: saal hm. Pediatrics. 2010 Mar;125(3):e543-9. doi: 10.1542/peds.2009-1656. Epub 2010 Feb 8. Pediatrics. 2010. PMID: 20142284

6

Epidemiology of hemimegalencephaly: a case series and review.

Tinkle BT, Schorry EK, Franz DN, Crone KR, Saal HM. Tinkle BT, et al. Among authors: saal hm. Am J Med Genet A. 2005 Dec 15;139(3):204-11. doi: 10.1002/ajmg.a.31024. Am J Med Genet A. 2005. PMID: 16283674 Review.

7

DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.

Rope AF, Cragun DL, Saal HM, Hopkin RJ. Rope AF, et al. Among authors: saal hm. J Pediatr. 2009 Oct;155(4):560-5. doi: 10.1016/j.jpeds.2009.04.010. J Pediatr. 2009. PMID: 19595366

8

Ullrich-Turner syndrome and neurofibromatosis-1.

Schorry EK, Lovell AM, Milatovich A, Saal HM. Schorry EK, et al. Among authors: saal hm. Am J Med Genet. 1996 Dec 30;66(4):423-5. doi: 10.1002/(SICI)1096-8628(19961230)66:4<423::AID-AJMG6>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8989459

9

Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome.

Hopkin RJ, Schorry EK, Bofinger M, Saal HM. Hopkin RJ, et al. Among authors: saal hm. J Pediatr. 2000 Aug;137(2):247-9. doi: 10.1067/mpd.2000.108272. J Pediatr. 2000. PMID: 10931419

10

CHARGE syndrome in the era of molecular diagnosis: Similar outcomes in those without coloboma or choanal atresia.

Simpson BN, Khattar D, Saal H, Prada CE, Choo D, Marcheschi L, Wiley S, Hopkin RJ. Simpson BN, et al. Eur J Med Genet. 2021 Jan;64(1):104103. doi: 10.1016/j.ejmg.2020.104103. Epub 2020 Nov 12. Eur J Med Genet. 2021. PMID: 33189935

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