Kamath BM - Search Results

1

Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3.

Leyva-Vega M, Gerfen J, Thiel BD, Jurkiewicz D, Rand EB, Pawlowska J, Kaminska D, Russo P, Gai X, Krantz ID, Kamath BM, Hakonarson H, Haber BA, Spinner NB. Leyva-Vega M, et al. Among authors: kamath bm. Am J Med Genet A. 2010 Apr;152A(4):886-95. doi: 10.1002/ajmg.a.33332. Am J Med Genet A. 2010. PMID: 20358598 Free PMC article.

2

Facial features in Alagille syndrome: specific or cholestasis facies?

Kamath BM, Loomes KM, Oakey RJ, Emerick KE, Conversano T, Spinner NB, Piccoli DA, Krantz ID. Kamath BM, et al. Am J Med Genet. 2002 Oct 1;112(2):163-70. doi: 10.1002/ajmg.10579. Am J Med Genet. 2002. PMID: 12244550

3

Supernumerary digital flexion creases: an additional clinical manifestation of Alagille syndrome.

Kamath BM, Loomes KM, Oakey RJ, Krantz ID. Kamath BM, et al. Am J Med Genet. 2002 Oct 1;112(2):171-5. doi: 10.1002/ajmg.10628. Am J Med Genet. 2002. PMID: 12244551

4

Craniosynostosis in Alagille syndrome.

Kamath BM, Stolle C, Bason L, Colliton RP, Piccoli DA, Spinner NB, Krantz ID. Kamath BM, et al. Am J Med Genet. 2002 Oct 1;112(2):176-80. doi: 10.1002/ajmg.10608. Am J Med Genet. 2002. PMID: 12244552

5

Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordance.

Kamath BM, Krantz ID, Spinner NB, Heubi JE, Piccoli DA. Kamath BM, et al. Am J Med Genet. 2002 Oct 1;112(2):194-7. doi: 10.1002/ajmg.10610. Am J Med Genet. 2002. PMID: 12244555

6

Consequences of JAG1 mutations.

Kamath BM, Bason L, Piccoli DA, Krantz ID, Spinner NB. Kamath BM, et al. J Med Genet. 2003 Dec;40(12):891-5. doi: 10.1136/jmg.40.12.891. J Med Genet. 2003. PMID: 14684686 Free PMC article.

7

Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality.

Kamath BM, Spinner NB, Emerick KM, Chudley AE, Booth C, Piccoli DA, Krantz ID. Kamath BM, et al. Circulation. 2004 Mar 23;109(11):1354-8. doi: 10.1161/01.CIR.0000121361.01862.A4. Epub 2004 Mar 1. Circulation. 2004. PMID: 14993126 Review.

8

Intracranial vascular abnormalities in patients with Alagille syndrome.

Emerick KM, Krantz ID, Kamath BM, Darling C, Burrowes DM, Spinner NB, Whitington PF, Piccoli DA. Emerick KM, et al. Among authors: kamath bm. J Pediatr Gastroenterol Nutr. 2005 Jul;41(1):99-107. doi: 10.1097/01.mpg.0000162776.67758.2f. J Pediatr Gastroenterol Nutr. 2005. PMID: 15990638

9

Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate.

Warthen DM, Moore EC, Kamath BM, Morrissette JJ, Sanchez-Lara PA, Piccoli DA, Krantz ID, Spinner NB. Warthen DM, et al. Among authors: kamath bm. Hum Mutat. 2006 May;27(5):436-43. doi: 10.1002/humu.20310. Hum Mutat. 2006. PMID: 16575836

10

SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.

Kamath BM, Thiel BD, Gai X, Conlin LK, Munoz PS, Glessner J, Clark D, Warthen DM, Shaikh TH, Mihci E, Piccoli DA, Grant SF, Hakonarson H, Krantz ID, Spinner NB. Kamath BM, et al. Hum Mutat. 2009 Mar;30(3):371-8. doi: 10.1002/humu.20863. Hum Mutat. 2009. PMID: 19058200 Free PMC article.

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