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Year | Number of Results |
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2014 | 1 |
2015 | 1 |
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Page 1
Molecular genetics of phenylketonuria and tetrahydrobiopterin deficiency in Jordan.
JIMD Rep. 2020 May 19;55(1):59-67. doi: 10.1002/jmd2.12130. eCollection 2020 Sep.
JIMD Rep. 2020.
PMID: 32905092
Free PMC article.
Identification and Characterization of BTD Gene Mutations in Jordanian Children with Biotinidase Deficiency.
Al-Eitan LN, Alqa'qa' K, Amayreh W, Khasawneh R, Aljamal H, Al-Abed M, Haddad Y, Rawashdeh T, Jaradat Z, Haddad H.
Al-Eitan LN, et al. Among authors: amayreh w.
J Pers Med. 2020 Jan 21;10(1):4. doi: 10.3390/jpm10010004.
J Pers Med. 2020.
PMID: 31973013
Free PMC article.
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Molecular analysis of LPIN1 in Jordanian patients with rhabdomyolysis.
Jaradat SA, Amayreh W, Al-Qa'qa' K, Krayyem J.
Jaradat SA, et al. Among authors: amayreh w.
Meta Gene. 2015 Dec 22;7:90-4. doi: 10.1016/j.mgene.2015.12.003. eCollection 2016 Feb.
Meta Gene. 2015.
PMID: 26909335
Free PMC article.
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Periodontal Manifestation of Type Ib Glycogen Storage Disease: A Rare Case Report.
Dababneh R, Shawabkeh A, Gharaibeh S, Khouri ZA, Amayreh W, Bissada NF.
Dababneh R, et al. Among authors: amayreh w.
Clin Adv Periodontics. 2020 Sep;10(3):150-154. doi: 10.1002/cap.10112. Epub 2020 Jul 28.
Clin Adv Periodontics. 2020.
PMID: 33460318
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Novel mutations in the SMPD1 gene in Jordanian children with Acid sphingomyelinase deficiency (Niemann-Pick types A and B).
Al-Eitan L, Alqa'qa' K, Amayreh W, Aljamal H, Khasawneh R, Al-Zoubi B, Okour I, Haddad A, Haddad Y, Haddad H.
Al-Eitan L, et al. Among authors: amayreh w.
Gene. 2020 Jul 15;747:144683. doi: 10.1016/j.gene.2020.144683. Epub 2020 Apr 18.
Gene. 2020.
PMID: 32311413
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Treatment of arginase deficiency revisited: guanidinoacetate as a therapeutic target and biomarker for therapeutic monitoring.
Amayreh W, Meyer U, Das AM.
Amayreh W, et al.
Dev Med Child Neurol. 2014 Oct;56(10):1021-4. doi: 10.1111/dmcn.12488. Epub 2014 May 10.
Dev Med Child Neurol. 2014.
PMID: 24814679
Free article.
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