Recent Publications on Ichthyosis: |  |
LC-MS/MS analysis of epoxyalcohols and epoxides of arachidonic acid and their oxygenation by recombinant CYP4F8 and CYP4F22.
CYP4F22 and CYP4F8 are expressed in epidermis, and mutations of CYP4F22...
Direct Link | 19th November, 2009
| Division of Biochemical Pharmacology, Department of Pharmaceutical
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Sjogren-Larsson syndrome in two brothers: a case report.
Sjogren-Larsson syndrome is a rare autosomal recessive disorder that was...
Direct Link | 18th November, 2009
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| The skin's barrier.
| 13th November, 2009
| Department of Dermatology, University Hospitals of Schleswig-Holstein,
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Sjogren-larsson syndrome: case report and review of neurologic abnormalities and ichthyosis.
INTRODUCTION: Sjogren-Larsson syndrome (SLS) is characterized by the triad...
Direct Link | 11th November, 2009
| Department of Neurology, Federal University of Sao Paulo, Sao Paulo,
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| [Serious cutaneous toxicity following ifosfamide, gemcitabine and vinorelbine therapy in a patient with relapsed Hodgkin lymphoma and ichthyosis]
| 11th November, 2009
| Univerzita Karlova v Praze, lekarska fakulta, I. interni klinika--klinika
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| Pityriasis rotunda.
| 7th November, 2009
| Department of Dermatology, New York University, USA.
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| Keratitis-ichthyosis-deafness (KID) syndrome.
| 7th November, 2009
| Department of Dermatology, New York University, USA.
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Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients.
Infants born with autosomal recessive congenital ichthyosis (ARCI) are...
Direct Link | 6th November, 2009
| Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
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Genotype-phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis.
Infants born with autosomal recessive congenital ichthyosis (ARCI) are...
Direct Link | 30th October, 2009
| Department of Dermatology, Our Lady's Children's Hospital, Crumlin, Dublin
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Successful treatment of Candida albicans septicemia in a preterm infant with severe congenital ichthyosis (Harlequin baby).
Candida infections are a major cause of fungal septicemia in neonates and...
Direct Link | 21st October, 2009
| Department of neonatology, Clinic for Child and Adolescent Medicine,
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Ichthyosis: clinical manifestations and practical treatment options.
Ichthyoses constitute a large group of cornification disorders that affect...
Direct Link | 15th October, 2009
| Department of Dermatology, University of Munster, Munster, Germany.
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Eccrine Squamous Metaplasia and Periadnexal Granulomas: New Cutaneous Histopathologic Findings in Cardiofaciocutaneous Syndrome.
Cardiofaciocutaneous syndrome is a rare genetic disorder characterized by...
Direct Link | 7th October, 2009
| From the Division of Pediatric Dermatology, Phoenix Children's Hospital,
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Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26.
The Keratitis-Ichthyosis-Deafness syndrome (KIDS) is an autosomal dominant...
Direct Link | 2nd October, 2009
| Department of Otolaryngology, Unfallkrankenhaus Berlin, Charite Medical
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Increased pachyonychia congenita severity in patients with concurrent keratin and filaggrin mutations.
Summary Pachyonychia congenita (PC), a rare autosomal-dominant keratin...
Direct Link | 30th September, 2009
| Department of Dermatology, Innsbruck Medical University, Anichstrasse 35,
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| A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome.
| 29th September, 2009
| National Skin Center, Institute of Medical Biology, 1 Mandalay Road,
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