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HELLENIC  ASSOCIATION  DERMATOLOGY - VENEREOLOGY

ICHTHYOSIS

  • Alpha hydroxyacid lotion
  • Altered Lamellar Body Secretion and Stratum Corneum Membrane Structure in Netherton Syndrome: Differentiation From Other Infantile Erythrodermas and Pathogenic Implications  Manige Fartasch, MD; Mary L. Williams, MD; Peter M. Elias, MD.Arch Dermatol. 1999;135:823-832
  • Autosomal dominant inheritance of HID syndrome (hystrix-like ichthyosis with deafness)  Arne KÖNIG, Wolfgang KÜSTER, Roswitha BERGER, Rudolf HAPPLE. Full text article
  • CAMPTODACTYLY-ICHTHYOSIS SYNDROME  OMIM
  • CATARACT AND CONGENITAL ICHTHYOSIS  OMIM
  • Clinical Delineation of the Keratitis-Ichthyosis-Deafness Syndrome
  • Clinical Trials: Ichthyosis  CenterWatch, Inc.
  • Dermatologie Online Atlas (DOIA) Erlangen: Ichthyosis congenita
  • Dermatology Online Atlas (DOIA) Erlangen: Ichthyosis Vulgaris
  • Disease Category Listing (279): Ichthyosis
  • ERYTHRODERMA DESQUAMATIVA OF LEINER  OMIM
  • Erythrodermia ichthyosiformis
  • Expression of transglutaminase 1 (transglutaminase K) in harlequin ichthyosis.M. Akiyama  , Soo-Youl Kim, Kozo Yoneda, Hiroshi Shimizu. Archives of Dermatological Research, Volume 289 Issue 2 (1997) pp 116-
  • F.I.R.S.T. - The Foundation for Ichthyosis and Related Skin Types
  • FIRST InfoF.I.R.S.T
  • Foundation for Ichthyosis and Related Skin Types
  • Foundation for Ichthyosis and Related Skin Types, Inc. (F.I.R.S.T.)   is the only national, non-profit oganization dedicated to helping families with the genetic skin diseases collectively called the ichthyoses. P.O. Box 669 Ardmore, PA 19003 Phone: 610-789-3995 FAX: 610-789-4366 Also: 800-545-3286
  • Glylorin Investigational Compound To Treat Ichthyosis Licensed to Glaxo  P\S\L Consulting Group Inc.
  • Hoe kan u ons en andere ichthyosispatiënten helpen?
  • CHTHYOSIFORM ERYTHRODERMA, BROCQ CONGENITAL, NONBULLOUS FORM  OMIM
  • CHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS  OMIM
  • Ichthyosis
  • ICHTHYOSIS AND MALE HYPOGONADISM  OMIM
  • ICHTHYOSIS BULLOSA OF SIEMENS IN NORFOLKS
  • Ichthyosis Bullosa of Siemens: A Topical Therapy Option  Gloria Sanclemente, MD; Rafael Falabella, MD; Carlos E. Escobar, MD; Jose A. Arroyave, BSC. Archives of Dermatology / volume:135 (page: 961)
  • Ichthyosis congenita
  • Ichthyosis Congenita
  • Ichthyosis congenita generalisata
  • ICHTHYOSIS CONGENITA IIB; ICR2B  OMIM
  • ICHTHYOSIS CONGENITA LAMELLAR EXFOLIATION OF NEWBORN;; DESQUAMATION OFNEWBORN;; COLLODION FETUS - IMAGE
  • ICHTHYOSIS CONGENITA OMIM
  • ICHTHYOSIS CONGENITA WITH BILIARY ATRESIA  OMIM
  • ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE  OMIM
  • Ichthyosis congenitaDOIA:
  • ICHTHYOSIS FOLLICULARIS, ATRICHIA, AND PHOTOPHOBIA SYNDROME  OMIM
  • ICHTHYOSIS HYSTRIX GRAVIOR  OMIM
  • ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE; IHCM  OMIM
  • Ichthyosis Info  F.I.R.S.T
  • Ichthyosis Informationis presented as a public service for benefit of the ichthyosis community.Ichthyosis.com
  • Ichthyosis lamellosa ("Collodium baby")
  • Ichthyosis PHOTO
  • ICHTHYOSIS PHOTOS
  • Ichthyosis PHOTOS  The Skin Site
  • Ichthyosis Simplex
  • Ichthyosis Treatment  Search Online Mendelian Inheritance in Man Data Base for Ichthyosis
  • Ichthyosis Vulgaris
  • Ichthyosis vulgaris nigricans
  • Ichthyosis vulgaris serpentina
  • Ichthyosis vulgaris simplex
  • ICHTHYOSIS VULGARIS  OMIM
  • Ichthyosis vulgaris, arm. PHOTO
  • Ichthyosis vulgarisDOIA:
  • ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION  OMIM
  • ICHTHYOSIS, BULLOUS TYPE  OMIM
  • ICHTHYOSIS, FOLLICULAR ATROPHODERMA, HYPOTRICHOSIS, AND HYPOHIDROSIS  OMIM
  • ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION  OMIM
  • ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS  OMIM
  • ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT FORM  OMIM
  • ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT  OMIM
  • ICHTHYOSIS, SPLIT HAIRS, AND AMINOACIDURIA  OMIM
  • ICHTHYOSIS, X-LINKED  OMIM
  • ICHTHYOSIS, X-LINKED, WITHOUT STEROID SULFATASE DEFICIENCY  OMIM
  • ICHTHYOSIS--CHEEK--EYEBROW SYNDROME  OMIM
  • IchthyosisIndiana Univ.
  • ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN OMIM
  • Index of /ichthyosis
  • Ittiosi
  • KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT  OMIM
  • Keratosis
  • KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA OMIM
  • Lamellar ichthyosis Library Pediatric Health Encyclopedia
  • Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35
  • Migratory Ichthyosiform Dermatosis With Type 2 Diabetes Mellitus and Insulin Resistance  Gil Yosipovitch, MD; Baruch Mevorah, MD; Michael David, MD; Maora F. Arch Dermatol. 135;1237-1242, October 1999,
  • Neostrata 15 AHA Body/Face Lotion
  • NETHERTON DISEASE OMIM
  • NORD - Ichthyosis, Tay Syndrome
  • Ocular Findings in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome    Claus Cursiefen, MD; Ursula Schlötzer-Schrehardt, PhD; Leonard M. Holbach, MD; Rudolf A. Pfeiffer, MD; Gottfried O. H.Naumann, MD. Arch Ophthalmol. 1999;117:681-684
  • ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS  OMIM
  • OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES
  • Registry F.I.R.S.T
  • Rezessive Ichthyosis congenita Typ II (Cholesterintyp)
  • Selbsthilfegruppe ICHTHYOSE "RIG-Bayern"
  • Selbsthilfegruppe Ichthyose Selbsthilfe Ichthyose e.V.  Schmollerstr.91 70378 Stuttgart
  • Selbsthilfegruppe Ichthyosis. Austria. Ichthyosis ist in der Medizin ein Fachausdruck für verschiedene, meist angeborene Hautkrankheit, die durch eine vermehrte Schuppung der Haut gekennzeichnet sind......
  • ServicesF.I.R.S.T
  • Short description of cell lines. Pathology: ichthyosis vulgaris *146700
  • Shwachman-Diamond-Syndrom
  • SJOGREN-LARSSON SYNDROME  OMIM
  • SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT  OMIM
  • Test:   Keratohyalin granules in Ichthyosis Vulgaris. Dermatology Laboratory Tests.   University of Rochester Medical Center Department of Dermatology
  • TGM1  Nucleotide substitutions (missense / nonsense)
  • The AnswerSleuth's Ichthyosis
  • The Ichthyoses are a family of genetic skin diseases characterized by excessively dry, thickened, scaling skin. Ichthyosis, often called "fish scale" disease, is disfiguring, often disabling and in some cases life threatening. Each year more than 16,000 babies are born in the U.S. with one of the estimated twenty (20) different forms of Ichthyosis.
  • The National Registry for Ichthyosis The National Registry for Ichthyosis and Related Disorders is supported by the National Institutes for Health.The success of the registry is critical for everyone affected by ichthyosis. If you, orsomeone you care about, has ichthyosis, please find out more about the registry and consider enrolling.
  • TRICHORRHEXIS NODOSA SYNDROME  OMIM
  • TRICHOTHIODYSTROPHY; TTD  OMIM
  • Types of Ichthyosis and Related Skin Diseases  F.I.R.S.T
  • Vitamin A and Genetic Disorders of Keratinization  Head of the project: Anders Vahlquist, Professor
  • VOHWINKEL SYNDROME, VARIANT FORM  OMIM
  • Was will die Selbsthilfegruppe Ichthyose?
  • Wat is Ichthyosis?
  • What is Ichthyosis?
  • What is it like to have ichthyosis?
  • Wat is vzw Ichthyosis Stichting België ?
  • X-chromosomal recessive Ichthyosis und Kallmann-Syndrom
  • Yahoo! Health>Diseases and Conditions>Ichthyosis
  • ZUNICH NEUROECTODERMAL SYNDROME  OMIM
  • G. Karakatsanis, Dermatologist.