Lestringant G - Search Results

1

SAM syndrome is characterized by extensive phenotypic heterogeneity.

Taiber S, Samuelov L, Mohamad J, Barak EC, Sarig O, Shalev SA, Lestringant G, Sprecher E. Taiber S, et al. Among authors: lestringant g. Exp Dermatol. 2018 Jul;27(7):787-790. doi: 10.1111/exd.13551. Exp Dermatol. 2018. PMID: 29604126 Review.

2

Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B.

Mohamad J, Samuelov L, Malki L, Peled A, Pavlovsky M, Malovitski K, Taiber S, Adir N, Rabinowitz T, Shomron N, Milner JD, Lestringant G, Sarig O, Sprecher E. Mohamad J, et al. Among authors: lestringant g. Clin Exp Dermatol. 2021 Jan;46(1):103-108. doi: 10.1111/ced.14384. Epub 2020 Sep 12. Clin Exp Dermatol. 2021. PMID: 32683719

3

Junctional epidermolysis bullosa in the Middle East: clinical and genetic studies in a series of consanguineous families.

Nakano A, Lestringant GG, Paperna T, Bergman R, Gershoni R, Frossard P, Kanaan M, Meneguzzi G, Richard G, Pfendner E, Uitto J, Pulkkinen L, Sprecher E. Nakano A, et al. Among authors: lestringant gg. J Am Acad Dermatol. 2002 Apr;46(4):510-6. doi: 10.1067/mjd.2002.119673. J Am Acad Dermatol. 2002. PMID: 11907499

4

Porokeratosis punctata palmaris et plantaris. A new entity?

Lestringant GG, Berge T. Lestringant GG, et al. Arch Dermatol. 1989 Jun;125(6):816-9. Arch Dermatol. 1989. PMID: 2525006

5

Tyrosinemia type II with incomplete Richner-Hanhart's syndrome.

Lestringant GG. Lestringant GG. Int J Dermatol. 1988 Jan-Feb;27(1):43-4. doi: 10.1111/j.1365-4362.1988.tb02336.x. Int J Dermatol. 1988. PMID: 2964425 No abstract available.

6

Functional implications of novel ADAM10 mutations in reticulate acropigmentation of Kitamura.

Ralser DJ, Lestringant GG, Du-Thanh A, Kokordelis P, Fischer J, Basmanav FBÜ, Wolf S, Thiele H, Altmüller J, Nürnberg P, Oji V, Fritz G, Frank J, Betz RC. Ralser DJ, et al. Among authors: lestringant gg. Br J Dermatol. 2017 Dec;177(6):e340-e343. doi: 10.1111/bjd.16024. Epub 2017 Nov 29. Br J Dermatol. 2017. PMID: 29192958 No abstract available.

7

Mal de Meleda.

Lestringant GG, Halawani NA, Zagzouk F. Lestringant GG, et al. Int J Dermatol. 1989 May;28(4):277-8. doi: 10.1111/j.1365-4362.1989.tb04827.x. Int J Dermatol. 1989. PMID: 2524451 No abstract available.

8

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates.

Eckl KM, Stevens HP, Lestringant GG, Westenberger-Treumann M, Traupe H, Hinz B, Frossard PM, Stadler R, Leigh IM, Nürnberg P, Reis A, Hennies HC. Eckl KM, et al. Among authors: lestringant gg. Hum Genet. 2003 Jan;112(1):50-6. doi: 10.1007/s00439-002-0838-8. Epub 2002 Oct 19. Hum Genet. 2003. PMID: 12483299

9

Rapid decay of alpha6 integrin caused by a mis-sense mutation in the propeller domain results in severe junctional epidermolysis bullosa with pyloric atresia.

Allegra M, Gagnoux-Palacios L, Gache Y, Roques S, Lestringant G, Ortonne JP, Meneguzzi G. Allegra M, et al. Among authors: lestringant g. J Invest Dermatol. 2003 Dec;121(6):1336-43. doi: 10.1111/j.1523-1747.2003.12625.x. J Invest Dermatol. 2003. PMID: 14675179 Free article.

10

Associations between the human insulin gene 5' VNTR and clinical variables of the renin-angiotensin system.

Frossard PM, Parvez SH, Lestringant GG, Kureshi NS. Frossard PM, et al. Among authors: lestringant gg. Neuro Endocrinol Lett. 2003 Oct;24(5):325-8. Neuro Endocrinol Lett. 2003. PMID: 14647005

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