Results 151 to 160 of about 888 (167)
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Lamellar icthyosis – A case report of a Nigerian child
Annals of Biomedical Sciences, 2018Lamellar Ichthyosis (LI) is an autosomal recessive disorder with an incidence of less than 1 in 3 blacks. Lamellaricthyosis is usually diagnosed based on the history of collodion membrane at birth and the characteristic appearance of scales especially on the skin.
Madubuko, C.R, Benson, A.
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Clinical picture: Acquired icthyosis: A paraneoplastic skin manifestation of Hodgkin's disease
200212
Rizos, E. +7 more
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Icthyosis uteri. A case report.
American journal of obstetrics and gynecology, 1998W T, PATTON, G V, SQUIRES
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Prenatal Diagnosis of Harlequin Icthyosis.
Narayana Medical Journal, 2020Venkatesh Manchikanti
exaly
Icthyosis Congenita-Harlequin type -A case report
2020K Prathibha, K S Kumaravel, S Gobinathan
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[HODGKIN'S DISEASE WITH ACQUIRED ICTHYOSIS].
Marseille medical, 1996R, POINSO +3 more
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Maternal Skin Allograft for Cicatricial Ectropion in Congenital Icthyosis
Ophthalmic Plastic and Reconstructive Surgery, 2010Santosh G Honavar
exaly

