Johnson MP - Search Results

1

Fetal cardiomyopathy in neurofibromatosis type I: Novel phenotype and review of the literature.

Ritter A, Cuddapah S, Degenhardt K, Kasperski S, Johnson MP, O'Connor MJ, Ahrens-Nicklas R. Ritter A, et al. Among authors: johnson mp. Am J Med Genet A. 2019 Jun;179(6):1042-1046. doi: 10.1002/ajmg.a.61123. Epub 2019 Mar 28. Am J Med Genet A. 2019. PMID: 30919579 Review.

2

Utility of fetal muscle biopsy for diagnosis of nemaline myopathy.

Kasperski SB, Brennan AM, Corteville JE, Finkel RS, Golden J, Johnson MP, Wilson RD. Kasperski SB, et al. Among authors: johnson mp. Fetal Diagn Ther. 2008;24(4):400-4. doi: 10.1159/000170095. Epub 2008 Nov 6. Fetal Diagn Ther. 2008. PMID: 18987477

3

Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.

Schindewolf E, Khalek N, Johnson MP, Gebb J, Coleman B, Crowley TB, Zackai EH, McDonald-McGinn DM, Moldenhauer JS. Schindewolf E, et al. Among authors: johnson mp. Am J Med Genet A. 2018 Aug;176(8):1735-1741. doi: 10.1002/ajmg.a.38665. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055034 Free PMC article.

4

Hypoplastic left heart syndrome and the nutmeg lung pattern in utero: a cause and effect relationship or prognostic indicator?

Saul D, Degenhardt K, Iyoob SD, Surrey LF, Johnson AM, Johnson MP, Rychik J, Victoria T. Saul D, et al. Among authors: johnson mp, johnson am. Pediatr Radiol. 2016 Apr;46(4):483-9. doi: 10.1007/s00247-015-3514-6. Epub 2015 Dec 21. Pediatr Radiol. 2016. PMID: 26691156

5

Thoracoamniotic shunts: fetal treatment of pleural effusions and congenital cystic adenomatoid malformations.

Wilson RD, Baxter JK, Johnson MP, King M, Kasperski S, Crombleholme TM, Flake AW, Hedrick HL, Howell LJ, Adzick NS. Wilson RD, et al. Among authors: johnson mp. Fetal Diagn Ther. 2004 Sep-Oct;19(5):413-20. doi: 10.1159/000078994. Fetal Diagn Ther. 2004. PMID: 15305098

6

Determinants of parental decisions after the prenatal diagnosis of Down syndrome.

Kramer RL, Jarve RK, Yaron Y, Johnson MP, Lampinen J, Kasperski SB, Evans MI. Kramer RL, et al. Among authors: johnson mp. Am J Med Genet. 1998 Sep 23;79(3):172-4. doi: 10.1002/(sici)1096-8628(19980923)79:3<172::aid-ajmg4>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9788556

7

Molecular cytogenetic analysis of a de novo 5q31q33 deletion associated multiple congenital anomalies: case report.

Kramer RL, Feldman B, Ebrahim SA, Kasperski SB, Johnson MP, Evans MI. Kramer RL, et al. Among authors: johnson mp. Am J Med Genet. 1999 Jan 15;82(2):143-5. Am J Med Genet. 1999. PMID: 9934978

8

Prenatal diagnosis of 46,XY/46,XX mosaicism: a case report.

Yaron Y, Feldman B, Kramer RL, Kasperski SB, Vo T, Feldman GL, Johnson MP, Evans MI, Ebrahim SA. Yaron Y, et al. Among authors: johnson mp. Am J Med Genet. 1999 May 7;84(1):12-4. Am J Med Genet. 1999. PMID: 10213039

9

Amnioinfusion in the evaluation of fetal obstructive uropathy: the effect of antibiotic prophylaxis on complication rates.

Feldman B, Hassan S, Kramer RL, Kasperski SB, Evans MI, Johnson MP. Feldman B, et al. Among authors: johnson mp. Fetal Diagn Ther. 1999 May-Jun;14(3):172-5. doi: 10.1159/000020913. Fetal Diagn Ther. 1999. PMID: 10364669

10

Cystic adenomatoid malformation of the lung: review of genetics, prenatal diagnosis, and in utero treatment.

Wilson RD, Hedrick HL, Liechty KW, Flake AW, Johnson MP, Bebbington M, Adzick NS. Wilson RD, et al. Among authors: johnson mp. Am J Med Genet A. 2006 Jan 15;140(2):151-5. doi: 10.1002/ajmg.a.31031. Am J Med Genet A. 2006. PMID: 16353256 Review.

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