Author/Creator: Melhem, Motasem - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Melhem, Motasem

1. ANGPTL8/Betatrophin R59W variant is associated with higher glucose level in non-diabetic Arabs living in Kuwaits. Issue 1 (December 2016)

Authors:: Abu-Farha, Mohamed; Melhem, Motasem; Abubaker, Jehad; Behbehani, Kazem; Alsmadi, Osama; Elkum, Naser
Journal:: Lipids in health and disease
Issue:: Volume 15:Issue 1(2016)
Page Start:: 1
Record Type:: Journal Article
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2. Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain. (March 2016)

Authors:: Jaradat, Saied A; Caccia, Sonia; Rawashdeh, Rifaat; Melhem, Motasem; Al-Hawamdeh, Ali; Carzaniga, Thomas; Haddad, Hazem
Journal:: Molecular immunology
Issue:: Volume 71(2016:Mar.)
Page Start:: 123
Record Type:: Journal Article
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3. Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain. (March 2016)

Authors:: Jaradat, Saied A; Caccia, Sonia; Rawashdeh, Rifaat; Melhem, Motasem; Al-Hawamdeh, Ali; Carzaniga, Thomas; Haddad, Hazem
Journal:: Molecular immunology
Issue:: Volume 71(2016:Mar.)
Page Start:: 123
Record Type:: Journal Article
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4. ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait. Issue 6 (25th February 2014)

Authors:: Behbehani, Raed; Melhem, Motasem; Alghanim, Ghazi; Behbehani, Kazem; Alsmadi, Osama
Journal:: British journal of ophthalmology
Issue:: Volume 98:Issue 6(2014)
Page Start:: 826
Record Type:: Journal Article
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5. Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia. (3rd January 2017)

Authors:: Melhem, Motasem; Abu‐Farha, Mohamed; Antony, Dinu; Madhoun, Ashraf Al; Bacchelli, Chiara; Alkayal, Fadi; AlKhairi, Irina; John, Sumi; Alomari, Mohamad; Beales, Phillip L.; Alsmadi, Osama
Journal:: European journal of haematology
Issue:: Volume 98:Number 3(2017:Mar.)
Page Start:: 218
Record Type:: Journal Article
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6. The TCN2 variant of rs9606756 [Ile23Val] acts as risk loci for obesity‐related traits and mediates by interacting with Apo‐A1. Issue 6 (17th April 2017)

Authors:: Hebbar, Prashantha; Alkayal, Fadi; Nizam, Rasheeba; Melhem, Motasem; Elkum, Naser; John, Sumi Elsa; Abufarha, Mohamed; Alsmadi, Osama; Thanaraj, Thangavel Alphonse
Journal:: Obesity
Issue:: Volume 25:Issue 6(2017)
Page Start:: 1098
Record Type:: Journal Article
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