skip to main content
Idioma:
Resultados 1 2 3 next page
Mostrar Somente
Refinado por: tipo de recurso: Reports remover Wiley-Blackwell Full Collection 2013 remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Use of a soluble epoxide hydrolase inhibitor as an adjunctive analgesic in a horse with laminitis
Use of a soluble epoxide hydrolase inhibitor as an adjunctive analgesic in a horse with laminitis
Material Type:
Report 		Adicionar ao Meu Espaço

Use of a soluble epoxide hydrolase inhibitor as an adjunctive analgesic in a horse with laminitis

Guedes, Alonso GP ; Morisseau, Christophe ; Sole, Albert ; Soares, Joao HN ; Ulu, Arzu ; Dong, Hua ; Hammock, Bruce D

Veterinary Anaesthesia and Analgesia, 2013, Vol.40 (4), p.440-448

Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
2
Treatment of Methotrexate Intoxication with Various Modalities of Continuous Extracorporeal Therapy and Glucarpidase
Treatment of Methotrexate Intoxication with Various Modalities of Continuous Extracorporeal Therapy and Glucarpidase
Material Type:
Report 		Adicionar ao Meu Espaço

Treatment of Methotrexate Intoxication with Various Modalities of Continuous Extracorporeal Therapy and Glucarpidase

Vilay, A. Mary ; Mueller, Bruce A. ; Haines, Hilary ; Alten, Jeffery A. ; Askenazi, David J.

Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 2010, Vol.30 (1), p.111-111

Oxford, UK: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
3
Digenic FLNA and UCHL1 variants resulting in a complex phenotype
Digenic FLNA and UCHL1 variants resulting in a complex phenotype
Material Type:
Report 		Adicionar ao Meu Espaço

Digenic FLNA and UCHL1 variants resulting in a complex phenotype

Pernice, Helena F ; O'Donnell, Luke F ; Rossor, Alexander M ; Laura, Matilde ; Record, Christopher J ; Skorupinska, Mariola ; Blake, Julian ; Poh, Roy ; Polke, James ; Reilly, Mary M

Journal of the peripheral nervous system : JPNS, 2024, Vol.29 (1), p.111-115

Texto completo disponível

Citações Citado por
4
Senescent case of cholesterol ester storage disease that progressed to liver cirrhosis with a novel mutation (N250H) of lysosomal acid lipase gene
Senescent case of cholesterol ester storage disease that progressed to liver cirrhosis with a novel mutation (N250H) of lysosomal acid lipase gene
Material Type:
Report 		Adicionar ao Meu Espaço

Senescent case of cholesterol ester storage disease that progressed to liver cirrhosis with a novel mutation (N250H) of lysosomal acid lipase gene

Kojima, Seiichiro ; Watanabe, Norihito ; Takashimizu, Shinji ; Kagawa, Tatehiro ; Shiraishi, Koichi ; Koizumi, Jun ; Hirabayashi, Ken-ichi ; Ohkubo, Tomoichi ; Kamiguchi, Hiroshi ; Tsuda, Michio ; Mine, Tetsuya

Hepatology Research, 2013, Vol.43 (12), p.1361-1367

Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
5
Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report
Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report
Material Type:
Report 		Adicionar ao Meu Espaço

Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report

Kuranobu, Naomi ; Murakami, Jun ; Okamoto, Ken ; Nishimura, Rei ; Murayama, Kei ; Takamura, Ayumi ; Umeda, Toshiko ; Eto, Yoshikatsu ; Kanzaki, Susumu

Hepatology Research, 2016, Vol.46 (5), p.477-482

Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
6
Melanoma arising in a nevus of Ito: novel genetic mutations and a review of the literature on cutaneous malignant transformation of dermal melanocytosis
Melanoma arising in a nevus of Ito: novel genetic mutations and a review of the literature on cutaneous malignant transformation of dermal melanocytosis
Material Type:
Report 		Adicionar ao Meu Espaço

Melanoma arising in a nevus of Ito: novel genetic mutations and a review of the literature on cutaneous malignant transformation of dermal melanocytosis

Tse, Julie Y. ; Walls, Brooke E. ; Pomerantz, Hyemin ; Yoon, Charles H. ; Buchbinder, Elizabeth I. ; Werchniak, Andrew E. ; Dong, Fei ; Lian, Christine G. ; Granter, Scott R.

Journal of Cutaneous Pathology, 2016, Vol.43 (1), p.57-63

Oxford, UK: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
7
Breast Necrosis after Chemotherapy for Recurrent Ovarian Cancer: Report of a Case and Review of the Literature
Breast Necrosis after Chemotherapy for Recurrent Ovarian Cancer: Report of a Case and Review of the Literature
Material Type:
Report 		Adicionar ao Meu Espaço

Breast Necrosis after Chemotherapy for Recurrent Ovarian Cancer: Report of a Case and Review of the Literature

Matloob, Reza ; Alikhasi, Afsaneh ; Shirkhoda, Mohammad ; Najafi, Massoome

The Breast Journal, 2015, Vol.21 (4), p.418-422

Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
8
Porokeratosis ptychotropica: a rare and evolving variant of porokeratosis
Porokeratosis ptychotropica: a rare and evolving variant of porokeratosis
Material Type:
Report 		Adicionar ao Meu Espaço

Porokeratosis ptychotropica: a rare and evolving variant of porokeratosis

Yeo, Jennifer ; Winhoven, Sandra ; Tallon, Ben

Journal of Cutaneous Pathology, 2013, Vol.40 (12), p.1042-1047

Oxford, UK: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
9
Sirenomelia after phenobarbital and carbamazepine therapy in pregnancy
Sirenomelia after phenobarbital and carbamazepine therapy in pregnancy
Material Type:
Report 		Adicionar ao Meu Espaço

Sirenomelia after phenobarbital and carbamazepine therapy in pregnancy

Tica, Oana Sorina ; Tica, Andrei Adrian ; Brailoiu, Cristina Gabriela ; Cernea, Nicolae ; Tica, Vlad Iustin

Birth Defects Research Part A: Clinical and Molecular Teratology, 2013, Vol.97 (6), p.425-428

Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
10
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: Further delineation of a critical region for the 14q32 deletion syndrome
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: Further delineation of a critical region for the 14q32 deletion syndrome
Material Type:
Report 		Adicionar ao Meu Espaço

A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: Further delineation of a critical region for the 14q32 deletion syndrome

Holder Jr, J. Lloyd ; Lotze, Timothy E. ; Bacino, Carlos ; Cheung, Sau-Wai

American Journal of Medical Genetics Part A, 2012, Vol.158A (8), p.1962-1966

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
Resultados 1 2 3 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (20)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.