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Refinado por: Base de dados/Biblioteca: Wiley-Blackwell Full Collection 2013 remover tipo de recurso: Reports remover
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1
Sporotrichosis masquerading as pyoderma gangrenosum
Sporotrichosis masquerading as pyoderma gangrenosum
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Sporotrichosis masquerading as pyoderma gangrenosum

Lima, R B ; Jeunon-Sousa, M A J ; Jeunon, T ; Oliveira, J C ; Oliveira, M M E ; Zancopé-Oliveira, R M ; Moraes, A C S

Journal of the European Academy of Dermatology and Venereology : JEADV, 2017, Vol.31 (12), p.e539-e541

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2
Nonclassic fibrodysplasia ossificans progressiva: A child from Angola with an ACVR1G328E variant
Nonclassic fibrodysplasia ossificans progressiva: A child from Angola with an ACVR1G328E variant
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Nonclassic fibrodysplasia ossificans progressiva: A child from Angola with an ACVR1G328E variant

Martín-García, Diana ; Towler, O Will ; Xu, Meiqi ; Alfonso-Hernández, Osmany ; Oliveira, Paula R ; Alonso-Clavo, Marleny ; Shore, Eileen M ; Kaplan, Frederick S

American journal of medical genetics. Part A, 2021, Vol.185 (8), p.2572-2575

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3
Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification
Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification
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Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification

Lemos, R R ; Oliveira, M F ; Oliveira, J R M

European journal of neurology, 2013, Vol.20 (3), p.e43-e44

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4
Sweet syndrome associated with sporotrichosis
Sweet syndrome associated with sporotrichosis
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Sweet syndrome associated with sporotrichosis

Freitas, D F S ; Valle, A C F ; Cuzzi, T ; Brandão, L G P ; Zancope-Oliveira, R M ; Galhardo, M C G

The British journal of dermatology, 2012, Vol.166 (1), p.212-213

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5
Transient amantadine-induced musical hallucinations in a patient with Parkinson's disease
Transient amantadine-induced musical hallucinations in a patient with Parkinson's disease
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Transient amantadine-induced musical hallucinations in a patient with Parkinson's disease

Gondim, Francisco de Assis Aquino ; Costa, Helida A ; Taunay, Tauily C D ; de Oliveira, Gisele R ; Ferreira, Jamile Magalhães ; Rola, Francisco H

Movement disorders : official journal of the Movement Disorder Society, 2010, Vol.25 (10), p.1505-1506

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6
Repeated syncopes, orthostatic hypotension and progressive visual impairment heralding the presentation of an occult gastric adenocarcinoma
Repeated syncopes, orthostatic hypotension and progressive visual impairment heralding the presentation of an occult gastric adenocarcinoma
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Repeated syncopes, orthostatic hypotension and progressive visual impairment heralding the presentation of an occult gastric adenocarcinoma

Gondim, F A A ; de Oliveira, G R ; Thomas, F P

European journal of neurology, 2007, Vol.14 (1), p.e44-e44

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7
Novel homozygous nonsense TMC8 mutation detected in patients with epidermodysplasia verruciformis from a Brazilian family
Novel homozygous nonsense TMC8 mutation detected in patients with epidermodysplasia verruciformis from a Brazilian family
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Novel homozygous nonsense TMC8 mutation detected in patients with epidermodysplasia verruciformis from a Brazilian family

Rady, P L ; De Oliveira, W R P ; He, Q ; Festa, C ; Rivitti, E A ; Tucker, S B ; Tyring, S K

The British journal of dermatology, 2007, Vol.157 (4), p.831-833

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8
Two case reports of cutaneous adverse reactions following hepatitis B vaccine: lichen planus and granuloma annulare
Two case reports of cutaneous adverse reactions following hepatitis B vaccine: lichen planus and granuloma annulare
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Two case reports of cutaneous adverse reactions following hepatitis B vaccine: lichen planus and granuloma annulare

Criado, PR ; De Oliveira Ramos, R ; Vasconcellos, C ; Jardim Criado, RF ; Valente, NYS

Journal of the European Academy of Dermatology and Venereology, 2004, Vol.18 (5), p.603-606

Oxford, UK: Blackwell Science Ltd

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9
A7445G mtDNA mutation present in a Portuguese family exhibiting hereditary deafness and palmoplantar keratoderma
A7445G mtDNA mutation present in a Portuguese family exhibiting hereditary deafness and palmoplantar keratoderma
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A7445G mtDNA mutation present in a Portuguese family exhibiting hereditary deafness and palmoplantar keratoderma

Caria, H ; Matos, T ; Oliveira-Soares, R ; Santos, AR ; Galhardo, I ; Soares-Almeida, L ; Dias, O ; Andrea, M ; Correia, C ; Fialho, G

Journal of the European Academy of Dermatology and Venereology, 2005, Vol.19 (4), p.455-458

Oxford, UK: Blackwell Science Ltd

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10
Treatment with pentoxifylline in Behçet's disease
Treatment with pentoxifylline in Behçet's disease
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Treatment with pentoxifylline in Behçet's disease

Oliveira-Soares, R ; Freitas, J P ; Sousa Ramalho, P ; Guerra Rodrigo, F

Journal of the European Academy of Dermatology and Venereology : JEADV, 2002, Vol.16 (2), p.181-182

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