Works matching AU Lestringant, G.

Results: 32

Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency).

Published in:

2000

By:

Sztriha, László;
Al-Gazali, Lihadh I;
Wanders, Ronald J A;
Ofman, Rob;
Nork, Michael;
Lestringant, Gilles G;
Sztriha, L;
Al-Gazali, L I;
Wanders, R J;
Ofman, R;
Nork, M;
Lestringant, G G

Publication type:

journal article

Aetiology of onychomycosis in Al Ain, United Arab Emirates.

Published in:

Mycoses, 1995, v. 38, n. 9/10, p. 421, doi. 10.1111/j.1439-0507.1995.tb00075.x

By:

Nsanze, H.;
Lestringant, G. G.;
Mustafa, N.;
Usmani, M. A.

Publication type:

Article

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

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 1, p. 103, doi. 10.1111/ced.14384

By:

Mohamad, J.;
Samuelov, L.;
Malki, L.;
Peled, A.;
Pavlovsky, M.;
Malovitski, K.;
Taiber, S.;
Adir, N.;
Rabinowitz, T.;
Shomron, N.;
Milner, J. D.;
Lestringant, G.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population.

Published in:

Experimental Dermatology, 2021, v. 30, n. 9, p. 1290, doi. 10.1111/exd.14345

By:

Mohamad, Janan;
Samuelov, Liat;
Malchin, Natalia;
Rabinowitz, Tom;
Assaf, Sari;
Malki, Liron;
Malovitski, Kiril;
Israeli, Shirli;
Grafi‐Cohen, Meital;
Bitterman‐Deutsch, Ora;
Molho‐Pessach, Vered;
Cohen‐Barak, Eran;
Bach, Gideon;
Garty, Ben Zion;
Bergman, Reuven;
Harel, Avikam;
Nanda, Arti;
Lestringant, Giles G.;
McGrath, John;
Shalev, Stavit

Publication type:

Article

Mai de Meleda: A Report of Four Cases from the United Arab Emirates.

Published in:

Pediatric Dermatology, 1997, v. 14, n. 3, p. 186, doi. 10.1111/j.1525-1470.1997.tb00234.x

By:

Lestringant, Gilles G.;
Frossard, Philippe M.;
Adeghate, Ernest;
Qayed, Khalil I.

Publication type:

Article

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

Published in:

Human Genetics, 2003, v. 112, n. 1, p. 50, doi. 10.1007/s00439-002-0838-8

By:

Eckl, Katja;
Stevens, Howard P.;
Lestringant, Gilles G.;
Westenberger-Treumann, Margaretha;
Traupe, Heiko;
Hinz, Britta;
Frossard, Philippe M.;
Stadler, Rudolf;
Leigh, Irene M.;
Nürnberg, Peter;
Reis, André;
Hennies, Hans

Publication type:

Article

The use of isotretinoin in the treatment of chronic deep dermatophyte infections.

Published in:

Journal of Dermatological Treatment, 1990, v. 1, n. 3, p. 169, doi. 10.3109/09546639009086724

By:

Lestringant, Gilles G.

Publication type:

Article

Genetic and Clinical Heterogeneity in Transgressive Palmoplantar Keratoderma.

Published in:

Journal of Investigative Dermatology, 2001, v. 116, n. 5, p. 825, doi. 10.1046/j.1523-1747.2001.01346-3.x

By:

Lestringant, Gilles G.;
Frossard, Philippe M.;
Eckl, Katja-Martina;
Reis, André;
Hennies, Hans Christian

Publication type:

Article

Reply.

Published in:

Journal of Investigative Dermatology, 2000, v. 115, n. 4, p. 762, doi. 10.1046/j.1523-1747.2000.00124-2.x

By:

Sprecher, Eli;
Lestringant, Gilles G.;
Szargel, Raymonde;
Bergman, Reuven;
Labay, Valentina;
Frossard, Philippe M.;
Friedman-Birnbaum, Rachel;
Cohen, Nadine

Publication type:

Article

Atrichia with Papular Lesions Resulting from a Nonsense Mutation Within the Human Hairless Gene.

Published in:

Journal of Investigative Dermatology, 1999, v. 113, n. 4, p. 687, doi. 10.1046/j.1523-1747.1999.00723.x

By:

Sprecher, Eli;
Lestringant, Gilles G.;
Szargel, Raymonde;
Bergman, Reuven;
Labay, Valentina;
Frossard, Philippe M.;
Friedman-Birnbaum, Rachel;
Cohen, Nadine

Publication type:

Article

Defective Integrin α6β4 Expression in the Skin of Patients With Junctional Epidermolysis Bullosa and Pyloric Atresia.

Published in:

Journal of Investigative Dermatology, 1996, v. 107, n. 3, p. 384, doi. 10.1111/1523-1747.ep12363370

By:

Brown, Tod A.;
Gil, Susana G.;
Sybert, Virginia P.;
Lestringant, Gilles G.;
Tadini, Gianluca;
Caputo, Ruggero;
Carter, William G.

Publication type:

Article

Haplotypes of the human renin gene associated with essential hypertension and stroke.

Published in:

Journal of Human Hypertension, 2001, v. 15, n. 1, p. 49, doi. 10.1038/sj.jhh.1001107

By:

Frossard, P M;
Malloy, M J;
Lestringant, G G;
Kane, J P

Publication type:

Article

Pathogenicity of POFUT1 in Dowling-Degos Disease: Additional Mutations and Clinical Overlap with Reticulate Acropigmentation of Kitamura.

Published in:

Journal of Investigative Dermatology, 2015, v. 135, n. 2, p. 615, doi. 10.1038/jid.2014.406

By:

Basmanav, F Buket;
Fritz, Günter;
Lestringant, Gilles G;
Pachat, Divya;
Hoffjan, Sabine;
Fischer, Johannes;
Wehner, Maria;
Wolf, Sabrina;
Thiele, Holger;
Altmüller, Janine;
Pulimood, Susanne A;
Rütten, Arno;
Kruse, Roland;
Hanneken, Sandra;
Frank, Jorge;
Danda, Sumita;
Bygum, Anette;
Betz, Regina C

Publication type:

Article

Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing.

Published in:

Journal of Investigative Dermatology, 2009, v. 129, p. 862, doi. 10.1038/jid.2008.311

By:

Alef, Thomas;
Torres, Serena;
Hausser, Ingrid;
Metze, Dieter;
Türsen, Ümit;
Lestringant, Gilles G.;
Hennies, Hans Christian

Publication type:

Article

Allergic contact dermatitis in the United Arab Emirates.

Published in:

International Journal of Dermatology, 1999, v. 38, n. 3, p. 181, doi. 10.1046/j.1365-4362.1999.00628.x

By:

Lestringant, Gilles G.;
Bener, Abdulbari;
Sawaya, Maha;
Galadari, Ibrahim H.;
Frossard, Philippe M.

Publication type:

Article

SEROLOGIC TESTS FOR TREPONEMATOSES IN THE UNITED ARAB EMIRATES.

Published in:

1996

By:

Nsanze, Herbert;
Lestringant, Giles G.;
Ameen, Abdul M.;
Lambert, Jean Marie;
Galadari, Ibrahim;
Usmani, Mohammed A.

Publication type:

Report

Practicing Dermatology in a Gulf Country.

Published in:

1991

By:

Goihman-Yahr, Mauricio;
Lestringant, Gilles G.

Publication type:

Letter

Tinea Capitis in the United Arab Emirates.

Published in:

International Journal of Dermatology, 1991, v. 30, n. 2, p. 127, doi. 10.1111/j.1365-4362.1991.tb04225.x

By:

Lestringant, Gilles G.;
Qayed, Khalil;
Blayney, Benedict

Publication type:

Article

Mai de Meleda.

Published in:

1989

By:

Goihman-Yahr, Mauricio;
Lestringant, Gilles G.;
Halawani, Nawal A.;
Zagzouk, Fayez

Publication type:

Letter

Deep Dermatophytosis to Trichophyton rubrum and T. verrucosum in an Immunosuppressed Patient.

Published in:

International Journal of Dermatology, 1988, v. 27, n. 10, p. 707, doi. 10.1111/j.1365-4362.1988.tb01269.x

By:

Lestringant, Gilles G.;
Lindley, Sheldon K.;
Hillsdon-Smith, Jeremy;
Bouix, Gerard

Publication type:

Article

Tyrosinemia Type II with Incomplete Richner-Hanhart's Syndrome.

Published in:

International Journal of Dermatology, 1988, v. 27, n. 1, p. 43, doi. 10.1111/j.1365-4362.1988.tb02336.x

By:

Lestringant, Gilles G.

Publication type:

Article

Correspondence.

Published in:

1994

By:

Yell, J. A.;
Burge, S. M.;
Balzan, M.;
Cacciottolo, J. M.;
Taïeb, A.;
Won, J. H.;
Ahn, S. K.;
Lee, S. H.;
Lee, W. S.;
Kim, S. C.;
Lestringant, G. G.;
Aal, G. A.;
Frossard, P. M.;
Qayed, K. I.;
Condon, C.;
Cotter, P.;
Lyons, J. F.;
Powles, A. V.;
Baker, B. S.;
Fry, L.

Publication type:

Letter

Human renin gene BglI dimorphism associated with hypertension in two independent populations.

Published in:

Clinical Genetics, 1999, v. 56, n. 6, p. 428, doi. 10.1034/j.1399-0004.1999.560604.x

By:

Frossard, Philippe M;
Lestringant, Gilles G;
Malloy, Mary J;
Kane, John P

Publication type:

Article

Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population.

Published in:

Clinical Genetics, 1998, v. 54, n. 4, p. 285, doi. 10.1034/j.1399-0004.1998.5440405.x

By:

Frossard, Philippe M;
Hill, Susan H;
Elshahat, Yassin I;
Obineche, Eniyoma N;
Bokhari, Awais M;
Lestringant, Gilles G;
John, Anne;
Abdulle, Abdishakur M

Publication type:

Article

Deletion polymorphism in the angiotensin-converting enzyme gene is not associated with hypertension in a Gulf Arab population.

Published in:

Clinical Genetics, 1997, v. 51, n. 3, p. 211, doi. 10.1111/j.1399-0004.1997.tb02455.x

By:

Frossard, P. M.;
Obineche, E. N.;
Elshahat, Y. I.;
Lestringant, G. G.

Publication type:

Article

Association between a dimorphic site on chromosome 12 and clinical diagnosis of hypertension in three independent populations.

Published in:

Clinical Genetics, 1995, v. 48, n. 6, p. 284, doi. 10.1111/j.1399-0004.1995.tb04110.x

By:

Frossard, Philippe M.;
Lestringant, Gilles G.

Publication type:

Article

MR and other imaging methods in the investigation of mycetomas.

Published in:

2001

By:

Czechowski, J.;
Nork, M.;
Haas, D.;
Lestringant, G.;
Ekelund, L.

Publication type:

journal article

Association Study Between the ANF Gene and Hypertension in a Gulf Arab Population*.

Published in:

American Journal of Hypertension, 1997, v. 10, n. 11, p. 1308, doi. 10.1016/S0895-7061(97)00303-8

By:

Frossard, Philippe M;
Obineche, Eniyoma N;
Lestringant, Gilles G;
Elshahat, Yassin I

Publication type:

Article

Identification of cystic fibrosis mutations in the United Arab Emirates.

Published in:

Human Mutation, 1998, v. 11, n. 5, p. 412, doi. 10.1002/(SICI)1098-1004(1998)11:5<412::AID-HUMU15>3.0.CO;2-O

By:

Frossard, Philippe M.;
Girodon, Emmanuelle;
Dawson, Kenneth P.;
Ghanem, Nada;
Plassa, François;
Lestringant, Gilles G.;
Goossens, Michel

Publication type:

Article

Respiratory symptoms and skin disorders in sewage workers.

Published in:

Journal of Environmental Science & Health. Part A. Toxic/Hazardous Substances & Environmental Engineering, 1998, v. 33, n. 8, p. 1657, doi. 10.1080/10934529809376810

By:

Bener, A.;
Lestringant, G. G.;
Dogan, M.;
Ibrahim, A.;
Pasha, M.A.H.;
Al‐Shadli, A.M.;
Islam, M.R.

Publication type:

Article

Respiratory symptoms and skin disorders in sewage workers

Published in:

Journal of Environmental Science & Health. Part A. Toxic/Hazardous Substances & Environmental Engineering, 1998, v. A33, n. 8, p. 1657

By:

Ibrahim, A.;
Bener, A.;
Islam, M. R.;
Dogan, M.;
Al-Shadli, A. M.;
Lestringant, G. G.;
Pasha, M. A. H.

Publication type:

Article

Functional implications of novel <italic>ADAM10</italic> mutations in reticulate acropigmentation of Kitamura.

Published in:

2017

By:

Ralser, D. J.;
Lestringant, G. G.;
Du‐Thanh, A.;
Kokordelis, P.;
Fischer, J.;
Basmanav, F.B.Ünalan;
Wolf, S.;
Thiele, H.;
Altmüller, J.;
Nürnberg, P.;
Oji, V.;
Fritz, G.;
Frank, J.;
Betz, R. C.

Publication type:

Letter to the Editor

Works matching AU Lestringant, G.

Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency).

Aetiology of onychomycosis in Al Ain, United Arab Emirates.

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

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population.

Mai de Meleda: A Report of Four Cases from the United Arab Emirates.

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

The use of isotretinoin in the treatment of chronic deep dermatophyte infections.

Genetic and Clinical Heterogeneity in Transgressive Palmoplantar Keratoderma.

Reply.

Atrichia with Papular Lesions Resulting from a Nonsense Mutation Within the Human Hairless Gene.

Defective Integrin α6β4 Expression in the Skin of Patients With Junctional Epidermolysis Bullosa and Pyloric Atresia.

Haplotypes of the human renin gene associated with essential hypertension and stroke.

Pathogenicity of POFUT1 in Dowling-Degos Disease: Additional Mutations and Clinical Overlap with Reticulate Acropigmentation of Kitamura.

Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing.

Allergic contact dermatitis in the United Arab Emirates.

SEROLOGIC TESTS FOR TREPONEMATOSES IN THE UNITED ARAB EMIRATES.

Practicing Dermatology in a Gulf Country.

Tinea Capitis in the United Arab Emirates.

Mai de Meleda.

Deep Dermatophytosis to <em>Trichophyton rubrum</em> and <em>T. verrucosum</em> in an Immunosuppressed Patient.

Tyrosinemia Type II with Incomplete Richner-Hanhart's Syndrome.

Correspondence.

Human renin gene BglI dimorphism associated with hypertension in two independent populations.

Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population.

Deletion polymorphism in the angiotensin-converting enzyme gene is not associated with hypertension in a Gulf Arab population.

Association between a dimorphic site on chromosome 12 and clinical diagnosis of hypertension in three independent populations.

MR and other imaging methods in the investigation of mycetomas.

Association Study Between the ANF Gene and Hypertension in a Gulf Arab Population<sup>*</sup>.

Identification of cystic fibrosis mutations in the United Arab Emirates.

Respiratory symptoms and skin disorders in sewage workers.

Respiratory symptoms and skin disorders in sewage workers

Functional implications of novel <italic>ADAM10</italic> mutations in reticulate acropigmentation of Kitamura.