Lin SP - Search Results

1

Tubulointerstitial nephritis associated with a novel mitochondrial point mutation.

Tzen CY, Tsai JD, Wu TY, Chen BF, Chen ML, Lin SP, Chen SC. Tzen CY, et al. Among authors: lin sp. Kidney Int. 2001 Mar;59(3):846-54. doi: 10.1046/j.1523-1755.2001.059003846.x. Kidney Int. 2001. PMID: 11231339 Free article.

2

Galloway-Mowat syndrome: a glomerular basement membrane disorder?

Lin CC, Tsai JD, Lin SP, Tzen CY, Shen EY, Shih CS. Lin CC, et al. Among authors: lin sp. Pediatr Nephrol. 2001 Aug;16(8):653-7. doi: 10.1007/s004670100628. Pediatr Nephrol. 2001. PMID: 11519896

3

Favorable outcome in a fetus with an early-onset extensive cystic hygroma colli and intralesional hemorrhage.

Chen CP, Wang W, Lin SP, Sheu JC, Tzen CY. Chen CP, et al. Among authors: lin sp. Am J Perinatol. 1998;15(11):601-5. doi: 10.1055/s-2007-994077. Am J Perinatol. 1998. PMID: 10064200

4

Glycogen storage disease type IV: a case report.

Chan YJ, Lin SP, Chen BF. Chan YJ, et al. Among authors: lin sp. Zhonghua Yi Xue Za Zhi (Taipei). 1999 Oct;62(10):743-7. Zhonghua Yi Xue Za Zhi (Taipei). 1999. PMID: 10533307

5

Juvenile nephronophthisis-medullary cystic disease complex: a family study.

Tsai JD, Lin SP, Huang FY, Hsu HC, Tsai TC. Tsai JD, et al. Among authors: lin sp. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 Mar-Apr;38(2):116-20. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997. PMID: 9151464

6

Perinatal findings in a male fetus with congenital megacystis and anorectal malformations.

Chen CP, Wang W, Lin SP, Sheu JC, Tsai JD. Chen CP, et al. Among authors: lin sp. Fetal Diagn Ther. 1998 Nov-Dec;13(6):348-51. doi: 10.1159/000020867. Fetal Diagn Ther. 1998. PMID: 9933817

7

Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).

Chen CP, Lin SP, Tzen CY, Hwu WL, Chern SR, Chuang CK, Chiang SS, Wang W. Chen CP, et al. Among authors: lin sp. Genet Couns. 2007;18(1):49-56. Genet Couns. 2007. PMID: 17515300

8

Progressive fetal axillary cystic lymphangioma with coexistent naevus flammeus.

Chen CP, Chen HC, Liu FF, Jan SW, Lin SP, Sheu JC, Chen BF. Chen CP, et al. Among authors: lin sp. Br J Dermatol. 1997 Jan;136(1):102-4. Br J Dermatol. 1997. PMID: 9039304

9

Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.

Chen CP, Lin SP, Chen M, Su YN, Chern SR, Wang TY, Liu YP, Tsai FJ, Lee CC, Chen YJ, Wang W. Chen CP, et al. Among authors: lin sp. Genet Couns. 2011;22(3):273-80. Genet Couns. 2011. PMID: 22029168

10

Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findings.

Chen CP, Lin SP, Chang TY, Tsai JD, Huang JK, Wang W. Chen CP, et al. Among authors: lin sp. Genet Couns. 2006;17(1):87-9. Genet Couns. 2006. PMID: 16719284 No abstract available.

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