Nishikawa T - Search Results

1

Prenatal diagnosis of tyrosinase-negative oculocutaneous albinism.

Shimizu H, Ishiko A, Kikuchi A, Akiyama M, Suzumori K, Nishikawa T. Shimizu H, et al. Among authors: nishikawa t. Lancet. 1992 Sep 19;340(8821):739-40. doi: 10.1016/0140-6736(92)92288-q. Lancet. 1992. PMID: 1355848 No abstract available.

2

Histology of fetal eyes with oculocutaneous albinism.

Akeo K, Shirai S, Okisaka S, Shimizu H, Miyata H, Kikuchi A, Nishikawa T, Suzumori K, Fujiwara T, Majima A. Akeo K, et al. Among authors: nishikawa t. Arch Ophthalmol. 1996 May;114(5):613-6. doi: 10.1001/archopht.1996.01100130605021. Arch Ophthalmol. 1996. PMID: 8619776

3

Epidermal melanocytes in normal and tyrosinase-negative oculocutaneous albinism fetuses.

Kikuchi A, Shimizu H, Nishikawa T. Kikuchi A, et al. Among authors: nishikawa t. Arch Dermatol Res. 1995;287(6):529-33. doi: 10.1007/BF00374071. Arch Dermatol Res. 1995. PMID: 7487137

4

Prenatal diagnosis of tyrosinase-negative oculocutaneous albinism by an electron microscopic dopa reaction test of fetal skin.

Shimizu H, Ishiko A, Kikuchi A, Akiyama M, Suzumori K, Nishikawa T. Shimizu H, et al. Among authors: nishikawa t. Prenat Diagn. 1994 Jun;14(6):442-50. doi: 10.1002/pd.1970140605. Prenat Diagn. 1994. PMID: 7937580

5

Prenatal diagnosis of oculocutaneous albinism by analysis of the fetal tyrosinase gene.

Shimizu H, Niizeki H, Suzumori K, Aozaki R, Kawaguchi R, Hikiji K, Nishikawa T. Shimizu H, et al. Among authors: nishikawa t. J Invest Dermatol. 1994 Jul;103(1):104-6. doi: 10.1111/1523-1747.ep12391833. J Invest Dermatol. 1994. PMID: 8027570 Free article.

6

Do pigmented naevi in albinism provide evidence of tyrosinase positivity?

Akiyama M, Shimizu H, Sugiura M, Nishikawa T. Akiyama M, et al. Among authors: nishikawa t. Br J Dermatol. 1992 Dec;127(6):649-53. doi: 10.1111/j.1365-2133.1992.tb14882.x. Br J Dermatol. 1992. PMID: 1476926

7

X-linked recessive inheritance in a family with isolated congenital alopecia.

Anzai H, Shimizu H, Nishikawa T. Anzai H, et al. Among authors: nishikawa t. Lancet. 1996 Feb 3;347(8997):337-8. doi: 10.1016/s0140-6736(96)90522-x. Lancet. 1996. PMID: 8569404 No abstract available.

8

Heterogeneous reactivity with LH7.2 and the first prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa among Japanese patients.

Shimizu H, Suzumori K, Nishikawa T. Shimizu H, et al. Among authors: nishikawa t. Dermatology. 1996;192(3):203-7. doi: 10.1159/000246366. Dermatology. 1996. PMID: 8726631 Review.

9

Prenatal diagnosis of epidermolysis bullosa: first successful trial in Asia.

Shimizu H, Onodera Y, Ikeda S, Ogawa H, Suzumori K, Nishikawa T. Shimizu H, et al. Among authors: nishikawa t. Dermatology. 1994;188(1):46-9. doi: 10.1159/000247085. Dermatology. 1994. PMID: 8305757

10

Absence of detectable alpha 6 integrin in pyloric atresia-junctional epidermolysis bullosa syndrome. Application for prenatal diagnosis in a family at risk for recurrence.

Shimizu H, Suzumori K, Hatta N, Nishikawa T. Shimizu H, et al. Among authors: nishikawa t. Arch Dermatol. 1996 Aug;132(8):919-25. Arch Dermatol. 1996. PMID: 8712842

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