CUTIS LAXA, CONGENITAL FORM WITH PULMONARY EMPHYSEMA: AN ULTRASTRUCTURAL STUDYLEDOUX CORBUSIER M.1983; JOURNAL OF CUTANEOUS PATHOLOGY; ISSN 0303-6987; DNK; DA. 1983; VOL. 10; NO 5; PP. 340-349; BIBL. 2 P.Article

PINGUECULA AND ACTINIC ELASTOSIS: AN ULSTRASTRUCTURAL STUDYLEDOUX CORBUSIER M; DANIS P.1979; J. CUTAN. PATHOL.; DNK; DA. 1979; VOL. 6; NO 5; PP. 404-413; BIBL. 2 P.Article

ALPHA ₁-ANTITRYPSIN DEFICIENCY AND SKIN ABNORMALITIES = ABSENCE D'ALPHA ₁ ANTITRYPSINE ET ANOMALIES CUTANEESLEDOUX CORBUSIER M; ACHTEN G.1975; J. CUTAN. PATHOL.; DENM.; DA. 1975; VOL. 2; NO 1; PP. 25-29; BIBL. 1P.Article

ELASTOSIS IN CHRONIC RADIODERMATITIS. AN ULTRASTRUCTURAL STUDY = L'ELASTOSE AU COURS DE LA RADIODERMITE CHRONIQUE. UNE ETUDE ULTRASTRUCTURALELEDOUX CORBUSIER M; ACHTEN G.1974; BRIT. J. DERMATOL.; G.B.; DA. 1974; VOL. 91; NO 3; PP. 287-295; BIBL. 1P.Article

Les élastolyses héréditaires = Inherited elastolysisLEDOUX-CORBUSIER, M.Dermatologica. 1985, Vol 171, Num 6, pp 407-418, issn 0011-9075Article

DEFICIENCE TOTALE EN ALPHA-I-ANTITRYPSINE CHEZ UN MALADE ATTEINT D'UN SYNDROME D'EHLERS-DANLOS.ACHTEN G; LEDOUX CORBUSIER M; SCHANDEVYL W et al.1976; ANN. DERMATOL. SYPHILIGR.; FR.; DA. 1976; VOL. 103; NO 4; PP. 403-411; ABS. ANGL.; BIBL. 2 P.Article

Autonomie nosologique et pathogénie des syndromes paranéoplasiques cutanés = Classification and pathogenesis of cutaneous paraneoplastic syndromesACHTEN, G; LEDOUX-CORBUSIER, M; GOENS, J et al.Annales de médecine interne (Paris). 1984, Vol 135, Num 8, pp 646-653, issn 0003-410XArticle

A new combination of tolnaphtate and methylpartricine (SPA-S-345, tritol) for mycotic skin infectionsLOWY, M; PARENT, D; LEDOUX-CORBUSIER, M et al.Mykosen. 1985, Vol 28, Num 9, pp 452-456, issn 0027-5557Article

Clinical and immunologic response to isoprinosine in alopecia areata and alopecia universalis: association with autoantibodiesLOWY, M; LEDOUX-CORBUSIER, M; ACHTEN, G et al.Journal of the American Academy of Dermatology. 1985, Vol 12, Num 1, pp 78-84, issn 0190-9622, 1Article

Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defectsBIVER, A; DE RIJCKE, S; TOPPET, V et al.Clinical genetics. 1994, Vol 45, Num 6, pp 318-322, issn 0009-9163Article

Dermatofibromes, élastomes et surdité: un nouveau cas de syndrome de Buschke-Ollendorff? = Dermatofibromas, elastoma and deafness: a new case of Buschke Ollendorff syndrome?PIETTE-BRION, B; LOWY-MOTULSKY, M; LEDOUX-CORBUSIER, M et al.Dermatologica. 1984, Vol 168, Num 5, pp 255-258, issn 0011-9075Article

Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibsVAN MALDERGEM, L; VAMOS, E; LAPORTE, M et al.American journal of medical genetics. 1988, Vol 31, Num 2, pp 455-464, issn 0148-7299Article

Syndrome d'immunodéficience acquise (AIDS) révélé par un herpès génital sévère: à propos de deux cas = Acquired immunodeficiency syndrome (AIDS) revealed by severe recurrent genetal herpes simplex. Two casesDE MAUBEUGE, J; MASCART-LEMONE, F; CLUMECK, N et al.Dermatologica. 1984, Vol 168, Num 3, pp 105-111, issn 0011-9075Article