Limwongse C - Search Results

1

Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand.

Kansuttiviwat C, Lertwilaiwittaya P, Roothumnong E, Nakthong P, Dungort P, Meesamarnpong C, Tansa-Nga W, Pongsuktavorn K, Wiboonthanasarn S, Tititumjariya W, Phuphuripan N, Lertbussarakam C, Wattanarangsan J, Sritun J, Punuch K, Kammarabutr J, Mutirangura P, Thongnoppakhun W, Limwongse C, Pithukpakorn M. Kansuttiviwat C, et al. Among authors: limwongse c. NPJ Genom Med. 2024 Feb 14;9(1):9. doi: 10.1038/s41525-024-00400-4. NPJ Genom Med. 2024. PMID: 38355628 Free PMC article.

2

Liddle's Syndrome: A Case Report.

Phoojaroenchanachai M, Buranakitjaroen P, Limwongse C. Phoojaroenchanachai M, et al. Among authors: limwongse c. J Med Assoc Thai. 2015 Oct;98(10):1035-40. J Med Assoc Thai. 2015. PMID: 26638596

3

Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation.

Kantaputra PN, van den Ouweland A, Sangruchi T, Limwongse C. Kantaputra PN, et al. Among authors: limwongse c. Am J Med Genet A. 2012 Jul;158A(7):1750-3. doi: 10.1002/ajmg.a.35422. Epub 2012 Jun 7. Am J Med Genet A. 2012. PMID: 22678692

4

Microcephaly-lymphedema-chorioretinal dysplasia: a unique genetic syndrome with variable expression and possible characteristic facial appearance.

Limwongse C, Wyszynski RE, Dickerman LH, Robin NH. Limwongse C, et al. Am J Med Genet. 1999 Sep 17;86(3):215-8. Am J Med Genet. 1999. PMID: 10482868

5

Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma.

Limwongse C, Schwartz S, Bocian M, Robin NH. Limwongse C, et al. Am J Med Genet. 1999 Jan 1;82(1):20-4. doi: 10.1002/(sici)1096-8628(19990101)82:1<20::aid-ajmg4>3.0.co;2-5. Am J Med Genet. 1999. PMID: 9916837 Review.

6

Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis.

Schrijver I, Karnsakul W, Limwongse C, Ramalingam S, Sankaran R, Gardner P, Moss R. Schrijver I, et al. Among authors: limwongse c. Am J Med Genet A. 2005 Feb 15;133A(1):103-5. doi: 10.1002/ajmg.a.30472. Am J Med Genet A. 2005. PMID: 15744829 No abstract available.

7

Iron overload in the Asian community.

Lok CY, Merryweather-Clarke AT, Viprakasit V, Chinthammitr Y, Srichairatanakool S, Limwongse C, Oleesky D, Robins AJ, Hudson J, Wai P, Premawardhena A, de Silva HJ, Dassanayake A, McKeown C, Jackson M, Gama R, Khan N, Newman W, Banait G, Chilton A, Wilson-Morkeh I, Weatherall DJ, Robson KJ. Lok CY, et al. Among authors: limwongse c. Blood. 2009 Jul 2;114(1):20-5. doi: 10.1182/blood-2009-01-199109. Epub 2009 Apr 2. Blood. 2009. PMID: 19342478 Free article.

8

Genetic testing for renal diseases: medical and ethical considerations.

Marsick R, Limwongse C, Kodish E. Marsick R, et al. Among authors: limwongse c. Am J Kidney Dis. 1998 Dec;32(6):934-45. doi: 10.1016/s0272-6386(98)70087-3. Am J Kidney Dis. 1998. PMID: 9856508 Review.

9

Effects of PCSK1 genetic variants on obesity among Thai children and their family members: in relation to health risk, and biochemical and anthropometric parameters.

Kulanuwat S, Phonrat B, Tungtrongchitr A, Limwongse C, Chongviriyaphan N, Tungtrongchitr R, Santiprabhob J. Kulanuwat S, et al. Among authors: limwongse c. Southeast Asian J Trop Med Public Health. 2014 Jan;45(1):214-25. Southeast Asian J Trop Med Public Health. 2014. PMID: 24964673

10

Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP).

Thongnoppakhun W, Limwongse C, Vareesangthip K, Sirinavin C, Bunditworapoom D, Rungroj N, Yenchitsomanus PT. Thongnoppakhun W, et al. Among authors: limwongse c. BMC Med Genet. 2004 Feb 3;5:2. doi: 10.1186/1471-2350-5-2. BMC Med Genet. 2004. PMID: 15018634 Free PMC article.

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