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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
O4 Familial juvenile idiopathic arthritis: clinical features and localization to chromosome 13q
O4 Familial juvenile idiopathic arthritis: clinical features and localization to chromosome 13q
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O4 Familial juvenile idiopathic arthritis: clinical features and localization to chromosome 13q

Al Mayouf Sulaiman, M ; Salma, M Wakil ; Rana, Al-Amr ; Osama, Alsmadi ; Dorota, Monies ; Brian, F Meyer

Indian journal of rheumatology, 2007, Vol.2 (3), p.S8-S9 [Periódico revisado por pares]

Elsevier B.V

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4
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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5
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
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Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T

Wakil, Salma M. ; Ramzan, Khushnooda ; Abuthuraya, Rula ; Hagos, Samya ; Al-Dossari, Haya ; Al-Omar, Rana ; Murad, Hatem ; Chedrawi, Aziza ; Al-Hassnan, Zuhair N. ; Finsterer, Josef ; Bohlega, Saeed

Gene, 2014-02, Vol.536 (1), p.217-220 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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6
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
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Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome

Monies, Dorota M ; Al-Hindi, Hindi N ; Al-Muhaizea, Mohamed A ; Jaroudi, Dyala J ; Al-Younes, Banan ; Naim, Ewa A ; Wakil, Salma M ; Meyer, Brian F ; Bohlega, Saeed

Neuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.353-359 [Periódico revisado por pares]

England: Elsevier B.V

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7
A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits
A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits
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A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits

Muiya, Nzioka P. ; Wakil, Salma ; Al-Najai, Mohammed ; Tahir, Asma I. ; Baz, Batoul ; Andres, Editha ; Al-Boudari, Olyan ; Al-Tassan, Nada ; Al-Shahid, Maie ; Meyer, Brian F. ; Dzimiri, Nduna

Gene, 2014-07, Vol.544 (2), p.152-158 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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8
Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
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Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2

Jan, Abid ; Basit, Sulman ; Wakil, Salma M ; Ramzan, Khushnooda ; Ahmad, Wasim

Journal of dermatological science, 2015-08, Vol.79 (2), p.173-175 [Periódico revisado por pares]

Netherlands: Elsevier Ireland Ltd

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9
Abnormalities of Skin and Cutaneous Appendages in Neuromuscular Disorders
Abnormalities of Skin and Cutaneous Appendages in Neuromuscular Disorders
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Abnormalities of Skin and Cutaneous Appendages in Neuromuscular Disorders

Finsterer, Josef, MD, PhD ; Wakil, Salma, PhD

Pediatric neurology, 2015-10, Vol.53 (4), p.301-308 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Stroke-like episodes, periepisodic seizures, and MELAS mutations
Stroke-like episodes, periepisodic seizures, and MELAS mutations
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Stroke-like episodes, periepisodic seizures, and MELAS mutations

Finsterer, Josef, Univ.Prof. DDr ; Wakil, Salma Majid, PhD

European journal of paediatric neurology, 2016 [Periódico revisado por pares]

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