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Genodermatosis
Keratosis Follicularis Spinulosa Decalvans in a Female Child- a Rare Presentation Chowdhury J1, Ghoshal L2, Bannerjee S3
Erythrokeratodermia Variabilis Et Progressiva Allelic to Oculo-Dento
Lymphatic Complaints in the Dermatology Clinic: an Osteopathic
Epidermolytic Hyperkeratosis with Ichthyosis Hystrix Geromanta Baleviciené, MD, Vilnius, Lithuania Robert A
Hereditary Hearing Impairment with Cutaneous Abnormalities
Mutation and Expression of Abca12in Keratosis Pilaris and Nevus
Generalized Epidermolytic Ichthyosis with Palmoplantar Hyperkeratosis
How to Deal with Skin Biopsy in an Infant with Blisters?
Postnatal Diagnosis of Harlequin Ichthyosis a Case Report
Hypohydrotic Ectodermal Dysplasia in Black Africans
Aagenaes Syndrome. See Cholestasis- Lymphedema Syndrome ABCB4
Poikiloderma with Neutropenia and Mastocytosis: a Case Report and a Review of Dermatological Signs
Hypohydrotic Ectodermal Dysplasia -A Case Report
Treatment of Palmoplantar Keratoderma with Continuous Infusion 5-Fluorouracil
This Month in Archives of Dermatology
Genodermatosis.Pdf (1.629Mb)
Epidermolysis Bullosa Simplex‑Dowling–Meara Mimicking Epidermolysis Bullosa Simplex with Mottled Pigmentation
Epidermolysis Bullosa Simplex with Mottled Pigmentation: a Family Report and Review
Top View
Darier's Disease Maps to Premature Keratinization, Presence of Villi, Corps, Ronds and Chromosome12q23-Q24.1
21 Genodermatoses
A Young Girl with Progressive Symmetrical Erythrokeratoderma and Short Height
Congenital Ichthyosis: an Overview of Current and Emerging Therapies*
Cutaneous Manifestations of Systemic Disease
Keratosis Follicularis Spinulosa Decalvans
**No Patient Handout Epidermolysis Bullosa Simplex
Erythrokeratoderma Variabilis in a 6 Year Old Child
Pigmentary Disorders: the Bizarre Truth of Pigmentary Disorders
Cutaneous Mastocytosis: a Case of Bullous Urticaria Pigmentosa
Keratosis Pilaris and Ulerythema Ophryogenes Associated with an 18P Deletion Caused by a Y/18 Translocation
Epidemiological, Clinical and Therapeutic Profile Of
Ebseq Epidermolysis Bullosa Genetic Testing by Next-Generation
Erythrokeratoderma Variabilis in Two Cases with Localized and Generalized Lesions
Hereditary Ichthyosis and Achieving the Oral Mucosa, Ret-Rospective
Dyskeratosis Congenita. Report of a Case with Literature Review
Epidermolytic Palmoplantar Keratoderma of Vörner-Case Report
X-Linked Ectodermal Dysplasia with Immunodeficiency Caused by NEMO Mutation Early Recognition and Diagnosis