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  1. No Access

    Reference Work Entry In depth

    Disorders of Keratinization

    Hereditary keratinization disorders are inherited skin diseases characterized by abnormal keratinization. The formation of an abnormal stratum corneum and hyperkeratotic skin lesions are the common characteris...

    Asmahane Souissi, Nourchène Toukabri… in Atlas of Dermatology, Dermatopathology and… (2022)

  2. No Access

    Reference Work Entry In depth

    Genodermatoses

    Genodermatoses comprise a clinically-heterogeneous group of mostly devastating disorders affecting the skin. The inherited monogenic skin disorders include blistering disorders, inflammatory disorders, and dis...

    Wissem Hafsi, Nourchène Toukabri… in Atlas of Dermatology, Dermatopathology and… (2022)

  3. No Access

    Living Reference Work Entry In depth

    Genodermatoses

    Genodermatoses comprise a clinically-heterogeneous group of mostly devastating disorders affecting the skin. The inherited monogenic skin disorders include blistering disorders, inflammatory disorders, and dis...

    Wissem Hafsi, Nourchène Toukabri… in Atlas of Dermatology, Dermatopathology and…

  4. No Access

    Living Reference Work Entry In depth

    Disorders of Keratinization

    Hereditary keratinization disorders are inherited skin diseases characterized by abnormal keratinization. The formation of an abnormal stratum corneum and hyperkeratotic skin lesions are the common characteris...

    Asmahane Souissi, Nourchène Toukebri… in Atlas of Dermatology, Dermatopathology and…

  5. Article

    Correction to: BRCA1 and BRCA2 Germline Mutation Analysis in Hereditary Breast/Ovarian Cancer Families from the Aures Region (Eastern Algeria): First Report

    The original version of this article unfortunately contained an error in the abstract section and Figure 2h image.

    Chiraz Mehemmai, Farid Cherbal, Yosr Hamdi… in Pathology & Oncology Research (2020)

    Download PDF (281 KB) View Article

  6. No Access

    Article

    BRCA1 and BRCA2 Germline Mutation Analysis in Hereditary Breast/Ovarian Cancer Families from the Aures Region (Eastern Algeria): First Report

    Breast cancer is currently the leading cause of cancer morbidity and mortality among Algerian women. In this study, we aimed to investigate the mutation spectrum of BRCA1 and BRCA2 genes in hereditary breast/ovar...

    Chiraz Mehemmai, Farid Cherbal, Yosr Hamdi… in Pathology & Oncology Research (2020)

  7. Article

    Open Access

    Adult gaucher disease in southern Tunisia: report of three cases

    Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far the most common form. It is characterized by variability in age of onset, clinical signs and progression. It is usually di...

    Faten Ben Rhouma, Faten Kallel, Rym Kefi, Wafa Cherif, Majdi Nagara… in Diagnostic Pathology (2012)

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