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1
Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis
Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis
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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

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2
Vertical transmission of hepatitis B virus despite maternal lamivudine therapy
Vertical transmission of hepatitis B virus despite maternal lamivudine therapy
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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

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3
Prevalence and profile of mutations associated with lamivudine therapy in Indian patients with chronic hepatitis B in the surface and polymerase genes of hepatitis B virus
Prevalence and profile of mutations associated with lamivudine therapy in Indian patients with chronic hepatitis B in the surface and polymerase genes of hepatitis B virus
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Prevalence and profile of mutations associated with lamivudine therapy in Indian patients with chronic hepatitis B in the surface and polymerase genes of hepatitis B virus

Wakil, Salma M. ; Kazim, Syed N. ; Khan, Luqman A. ; Raisuddin, Sheikh ; Parvez, Mohammad K. ; Guptan, Rajkumar C. ; Thakur, Varsha ; Hasnain, Seyed E. ; Sarin, Shiv K.

Journal of medical virology, 2002-11, Vol.68 (3), p.311-318 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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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
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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

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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
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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

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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 ( )
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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

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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
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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

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8
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Wakil, Salma M ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair N

European journal of medical genetics, 2013-01, Vol.56 (1), p.43-45 [Periódico revisado por pares]

Netherlands: Elsevier Masson SAS

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9
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
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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

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10
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
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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

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