skip to main content
Idioma:
Resultados 1 2 3 4 next page
Refinado por: assunto: Female remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis
Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis

KAPOOR, D ; GUPTAN, R. C ; WAKIL, S. M ; KAZIM, S. N ; KAUL, R ; AGARWAL, S. R ; RAISUDDIN, S ; HASNAIN, S. E ; SARIN, S. K

Journal of hepatology, 2000-08, Vol.33 (2), p.308-312 [Periódico revisado por pares]

Oxford: Elsevier

Texto completo disponível

Citações Citado por
2
Vertical transmission of hepatitis B virus despite maternal lamivudine therapy
Vertical transmission of hepatitis B virus despite maternal lamivudine therapy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Vertical transmission of hepatitis B virus despite maternal lamivudine therapy

Kazim, Syed N ; Wakil, Salma M ; Khan, Luqman A ; Hasnain, Seyed E ; Sarin, Shiv K

The Lancet (British edition), 2002-04, Vol.359 (9316), p.1488-1489 [Periódico revisado por pares]

London: Elsevier Ltd

Texto completo disponível

Citações Citado por
3
The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population
The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population
Material Type:
Artigo 		Adicionar ao Meu Espaço

The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population

Wakil, Salma M ; Al-Rubeaan, Khalid ; Alsmadi, Osama ; Imtiaz, Faiqa ; Carroll, Pamela ; Rajab, Mohammed ; Al-Katari, Shaden ; Al-Katari, Mohammed ; Meyer, Brian F

Diabetes care, 2006-01, Vol.29 (1), p.171-172 [Periódico revisado por pares]

United States

Texto completo disponível

Citações Citado por
4
Phenotypic variation and allelic heterogeneity in young patients with papillon-lefevre syndrome
Phenotypic variation and allelic heterogeneity in young patients with papillon-lefevre syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Phenotypic variation and allelic heterogeneity in young patients with papillon-lefevre syndrome

ULLRRO, Christer ; EL-SAMADI, Safia ; BOUMAH, Christine ; AL-YOUSEF, Nujoud ; WAKIL, Salma ; TWETMAN, Svante ; ALFADLEY, Abdullah ; THESTRUP-PEDERSEN, Kristian ; MEYER, Brian

Acta dermato-venereologica, 2006-01, Vol.86 (1), p.3-7 [Periódico revisado por pares]

Uppsala: Acta dermato-venereologica

Texto completo disponível

Citações Citado por
5
Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes
Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes

Alsmadi, Osama ; Al-Rubeaan, Khalid ; Wakil, Salma M. ; Imtiaz, Faiqa ; Mohamed, Gamal ; Al-Saud, Haya ; Al-Saud, Nouran Abu ; Aldaghri, Nasser ; Mohammad, Shahinaz ; Meyer, Brian F

Diabetes/metabolism research and reviews, 2008-02, Vol.24 (2), p.137-140 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

Texto completo disponível

Citações Citado por
6
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )
Material Type:
Artigo 		Adicionar ao Meu Espaço

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )

ALSMADI, Osama ; MEYER, Brian F ; ALKURAYA, Fowzan ; WAKIL, Salma ; ALKAYAL, Fadi ; AL-SAUD, Haya ; RAMZAN, Khushnooda ; AL-SAYED, Moeenaldeen

European journal of human genetics : EJHG, 2009-01, Vol.17 (1), p.14-21 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

Texto completo disponível

Citações Citado por
7
Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients
Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients

Alsum, Zobaida ; Hawwari, Abbas ; Alsmadi, Osama ; Al-Hissi, Safa ; Borrero, Esteban ; Abu-staiteh, Asma’ ; Khalak, Hanif G. ; Wakil, Salma ; Eldali, Abdelmoneim M. ; Arnaout, Rand ; Al-ghonaium, Abdulaziz ; Al-Muhsen, Saleh ; Al-Dhekri, Hasan ; Al-Saud, Bandar ; Al-Mousa, Hamoud

Journal of clinical immunology, 2013, Vol.33 (1), p.55-67 [Periódico revisado por pares]

Boston: Springer US

Texto completo disponível

Citações Citado por
8
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
Material Type:
Artigo 		Adicionar ao Meu Espaço

New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3

Alshahid, Maie ; Wakil, Salma M ; Al-Najai, Mohammed ; Muiya, Nzioka P ; Elhawari, Samar ; Gueco, Daisy ; Andres, Editha ; Hagos, Samia ; Mazhar, Nejat ; Meyer, Brian F ; Dzimiri, Nduna

Human genomics, 2013-06, Vol.7 (1), p.15-15, Article 15 [Periódico revisado por pares]

England: BioMed Central

Texto completo disponível

Citações Citado por
9
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders

Muiya, Nzioka P ; Wakil, Salma M ; Tahir, Asma I ; Hagos, Samya ; Najai, Mohammed ; Gueco, Daisy ; Al-Tassan, Nada ; Andres, Editha ; Mazher, Nejat ; Meyer, Brian F ; Dzimiri, Nduna

Human genomics, 2013-12, Vol.7 (1), p.25-25, Article 25 [Periódico revisado por pares]

England: BioMed Central

Texto completo disponível

Citações Citado por
10
A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24
A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24
Material Type:
Artigo 		Adicionar ao Meu Espaço

A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24

Wakil, Salma M. ; Muiya, Nzioka P. ; Tahir, Asma I. ; Al-Najai, Mohammed ; Baz, Batoul ; Andres, Editha ; Mazhar, Nejat ; Al Tassan, Nada ; Alshahid, Maie ; Meyer, Brian F. ; Dzimiri, Nduna Letizia, Claudio

Disease markers, 2014-01, Vol.2014, p.291419-10 [Periódico revisado por pares]

United States: Hindawi Publishing Corporation

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Data de Publicação 

De até
Refinar
  1. Antes de2002  (2)
  2. 2002Até2007  (3)
  3. 2008Até2012  (2)
  4. 2013Até2015  (13)
  5. Após 2015  (15)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.