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Refinado por: Base de dados/Biblioteca: Wiley-Blackwell Full Collection 2009 remover tipo de recurso: Reports remover
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1
Clinical and dermoscopic features of common warts
Clinical and dermoscopic features of common warts
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Clinical and dermoscopic features of common warts

Li, X ; Yu, J ; Thomas, S ; Lee, K ; Soyer, H P

Journal of the European Academy of Dermatology and Venereology : JEADV, 2017, Vol.31 (7), p.e308-e310

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2
A case of subcutaneous dirofilariasis presenting in the UK: an unexpected finding
A case of subcutaneous dirofilariasis presenting in the UK: an unexpected finding
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A case of subcutaneous dirofilariasis presenting in the UK: an unexpected finding

Coelho, R R ; Tsigka, A ; Lee, K Y ; Grattan, C E H

Clinical and experimental dermatology, 2015, Vol.40 (4), p.449-451

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3
Intracostal neuralgia as a previously undescribed symptom of Schnitzler's syndrome
Intracostal neuralgia as a previously undescribed symptom of Schnitzler's syndrome
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Intracostal neuralgia as a previously undescribed symptom of Schnitzler's syndrome

Lee, K Y C ; Grattan, C E H

The British journal of dermatology, 2012, Vol.167 (6), p.1392-1393

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4
Acute generalized exanthematous pustulosis induced by a digestive enzyme drug, Festal
Acute generalized exanthematous pustulosis induced by a digestive enzyme drug, Festal
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Acute generalized exanthematous pustulosis induced by a digestive enzyme drug, Festal

Lee, S K ; Kim, M S ; Lee, U H

Clinical and experimental dermatology, 2018, Vol.43 (3), p.321-323

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5
Acquired von Willebrand syndrome in paediatric patients with congenital heart disease: challenges in the diagnosis and management of this rare condition
Acquired von Willebrand syndrome in paediatric patients with congenital heart disease: challenges in the diagnosis and management of this rare condition
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Acquired von Willebrand syndrome in paediatric patients with congenital heart disease: challenges in the diagnosis and management of this rare condition

Avila, M L ; Lee, K-J ; Bouskill, V ; Rand, M L ; James, P ; Carcao, M

Haemophilia : the official journal of the World Federation of Hemophilia, 2015, Vol.21 (1), p.e89-e92

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6
Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity
Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity
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Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity

Lee, K-E ; Ko, J ; Le, C G Tran ; Shin, T J ; Hyun, H-K ; Lee, S-H ; Kim, J-W

Clinical genetics, 2015, Vol.87 (1), p.90-92

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7
Successful treatment of vitiligo in a 6-year-old child by topical anaesthesia and epidermal grafting
Successful treatment of vitiligo in a 6-year-old child by topical anaesthesia and epidermal grafting
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Successful treatment of vitiligo in a 6-year-old child by topical anaesthesia and epidermal grafting

Lee, K-J ; Lee, J-H ; Lee, D-Y

Journal of the European Academy of Dermatology and Venereology : JEADV, 2009, Vol.23 (7), p.859-860

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8
The recommended dose of ertapenem poses a potential risk for central nervous system toxicity in haemodialysis patients - case reports and literature reviews
The recommended dose of ertapenem poses a potential risk for central nervous system toxicity in haemodialysis patients - case reports and literature reviews
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The recommended dose of ertapenem poses a potential risk for central nervous system toxicity in haemodialysis patients - case reports and literature reviews

Lee, K.-H. ; Ueng, Y.-F. ; Wu, C.-W. ; Chou, Y.-C. ; Ng, Y.-Y. ; Yang, W.-C.

Journal of Clinical Pharmacy and Therapeutics, 2015, Vol.40 (2), p.240-244

Blackwell Publishing Ltd

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9
A case of chromonychia with hyperbilirubinemia
A case of chromonychia with hyperbilirubinemia
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A case of chromonychia with hyperbilirubinemia

Roh, M ; Lee, J ; Lee, K

Journal of the European Academy of Dermatology and Venereology : JEADV, 2007, Vol.21 (1), p.127-128

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10
A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families
A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families
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A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families

Ahmad, F ; Ansar, M ; Mehmood, S ; Izoduwa, A ; Lee, K ; Nasir, A ; Abrar, M ; Ullah, A ; Aziz, A ; Smith, J D ; Shendure, J ; Bamshad, M J ; Nicekrson, D A ; Santos-Cortez, R L P ; Leal, S M ; Ahmad, W

Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Vol.30 (12), p.e210-e213

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