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Arif, T. and Adil, M. and Amin, S.S. (2018) Congenital atrichia with papular lesions: A rare cause of irreversible childhood alopecia. Acta Dermatovenerologica Alpina, Pannonica et Adriatica, 27 (1). pp. 35-36. ISSN 13184458
Arif, T. and Amin, S.S. and Adil, M. and Mohtashim, M. (2017) Diffuse palmoplantar keratoderma, onychodystrophy, universal hypotrichosis and cysts. Acta Dermatovenerologica Croatica, 25 (2). pp. 161-163. ISSN 1330027X
Arif, T. and Adil, M. and Amin, S.S. and Tahseen, M and Dorjay, K. and Mohtashim, M and Singh, M. and Bansal, R. and Raj, D. (2017) Erythromelanosis follicularis faciei et colli: A clinicoepidemiologic study. Pediatric Dermatology. ISSN 7368046
Arif, T. and Adil, M and Amin, S.S. and Dorjay, K. and Mohtashim, M. (2017) Late onset bilateral angioma serpiginosum involving upper limbs in a male: A rare presentation [Rzadki przypadek naczyniaka pełzakowatego o późnym początku z obustronnym zajȩciem kończyn górnych u pacjenta płci mȩskiej]. Przeglad Dermatologiczny, 104 (3). pp. 348-351. ISSN 332526
Arif, T. and Adil, M. and Amin, S.S. (2017) Neurofibromatosis-1 and zosteriform nevus spilus: A very rare clinical coexistence. Journal of Pakistan Association of Dermatologists, 27 (1). pp. 89-90. ISSN 15609014
Adil, M. and Amin, S.S. and Arif, T. (2017) Nicolau’s syndrome: A rare but preventable iatrogenic disease. Acta Dermatovenerologica Croatica, 25 (3). pp. 251-253. ISSN 1330027X
Arif, T. and Adil, M. and Amin, S.S. and Dorjay, K. (2017) Transgrediens et progrediens palmoplantar keratoderma: A case of Greither's disease. Przeglad Dermatologiczny, 104 (1). pp. 66-67. ISSN 332526
Arif, T. and Adil, M. and Amin, S.S. and Dorjay, K. (2017) An observation of autosomal recessive hyper-IgE syndrome: A rare case report [Autosomalny recesywny zespół hiper-IgE - opis rzadkiego przypadku]. Przeglad Dermatologiczny, 104 (6). pp. 676-679. ISSN 332526
