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J Arata

Showing results (121-130 of 164) with videos related to

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The Journal of Dermatology|October 1, 1989
Congenital alveolar rhabdomyosarcoma presenting as a blueberry muffin babyN Kitagawa, J Arata, Y Ohtsuki, et al.
Nihon Hifuka Gakkai Zasshi. the Japanese Journal of Dermatology|August 1, 1990
[Angiolymphoid hyperplasia with eosinophilia--report of a case with reference to the vascular changes and cell infiltrates in this disease]Y Nagao, J Tada, H Akiyama, et al.
Nihon Hifuka Gakkai Zasshi. the Japanese Journal of Dermatology|November 1, 1990
[Combination effects of fosfomycin and other oral antimicrobial agents against methicillin-resistant Staphylococcus aureus]H Akiyama, T Yamada, K Shimoe, et al.
European Journal of Dermatology : EJD|March 6, 1999
Hyperimmunoglobin E syndrome: a sign of TH1/TH2 imbalance?Y Shirafuji, H Matsuura, A Sato, et al.
The British Journal of Dermatology|July 24, 2004
Lichen planus pemphigoides and multiple keratoacanthomas associated with colon adenocarcinomaT Hamada, W Fujimoto, F Okazaki, et al.
The Journal of Hand Surgery|September 19, 2001
The palmar pocket method: an adjunct to the management of zone I and II fingertip amputationsJ Arata, K Ishikawa, H Soeda, et al.
The Journal of Clinical Investigation|April 1, 1991
Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptideA Tanoue, F Endo, I Akaboshi, et al.
Journal of the American Academy of Dermatology|April 3, 1999
Anti-epiligrin cicatricial pemphigoid with IgG autoantibodies to the beta and gamma subunits of laminin 5W Fujimoto, Y Toi, F Okazaki, et al.
Journal of the American Academy of Dermatology|May 1, 1991
Giant neuroendocrine (Merkel cell) carcinoma of the skinJ Tada, Y Toi, T Yamada, et al.
Journal of the American Academy of Dermatology|June 19, 1998
Pachyonychia congenita type 2: keratin 17 mutation in a Japanese caseW Fujimoto, G Nakanishi, S Hirakawa, et al.
Pageof 17

Showing results (121-130 of 164) with videos related to

Sort By:
Pageof 17
The Journal of Dermatology|October 1, 1989
Congenital alveolar rhabdomyosarcoma presenting as a blueberry muffin babyN Kitagawa, J Arata, Y Ohtsuki, et al.
Nihon Hifuka Gakkai Zasshi. the Japanese Journal of Dermatology|August 1, 1990
[Angiolymphoid hyperplasia with eosinophilia--report of a case with reference to the vascular changes and cell infiltrates in this disease]Y Nagao, J Tada, H Akiyama, et al.
Nihon Hifuka Gakkai Zasshi. the Japanese Journal of Dermatology|November 1, 1990
[Combination effects of fosfomycin and other oral antimicrobial agents against methicillin-resistant Staphylococcus aureus]H Akiyama, T Yamada, K Shimoe, et al.
European Journal of Dermatology : EJD|March 6, 1999
Hyperimmunoglobin E syndrome: a sign of TH1/TH2 imbalance?Y Shirafuji, H Matsuura, A Sato, et al.
The British Journal of Dermatology|July 24, 2004
Lichen planus pemphigoides and multiple keratoacanthomas associated with colon adenocarcinomaT Hamada, W Fujimoto, F Okazaki, et al.
The Journal of Hand Surgery|September 19, 2001
The palmar pocket method: an adjunct to the management of zone I and II fingertip amputationsJ Arata, K Ishikawa, H Soeda, et al.
The Journal of Clinical Investigation|April 1, 1991
Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptideA Tanoue, F Endo, I Akaboshi, et al.
Journal of the American Academy of Dermatology|April 3, 1999
Anti-epiligrin cicatricial pemphigoid with IgG autoantibodies to the beta and gamma subunits of laminin 5W Fujimoto, Y Toi, F Okazaki, et al.
Journal of the American Academy of Dermatology|May 1, 1991
Giant neuroendocrine (Merkel cell) carcinoma of the skinJ Tada, Y Toi, T Yamada, et al.
Journal of the American Academy of Dermatology|June 19, 1998
Pachyonychia congenita type 2: keratin 17 mutation in a Japanese caseW Fujimoto, G Nakanishi, S Hirakawa, et al.
Pageof 17