Forough Sargolzaeiaval

Title(s)Resident Physician, Pathology
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
La Jolla CA 92093
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Reconstruction of mandibular defects using synthetic octacalcium phosphate combined with bone matrix gelatin in rat model. Dent Res J (Isfahan). 2020 Jan-Feb; 17(1):10-18. Sargolzaei-Aval F, Saberi EA, Arab MR, Sargolzaei N, Zare E, Shahraki H, Sanchooli T, Sargolzaeiaval F, Arab M. PMID: 32055288.
      View in: PubMed   Mentions: 1  
    2. Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP Synthesis. DNA Cell Biol. 2020 Jan; 39(1):50-56. Zhang J, Hou D, Annis J, Sargolzaeiaval F, Appelbaum J, Takahashi E, Martin GM, Herr A, Oshima J. PMID: 31750734.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    3. Histomorphometric Analysis of Newly-formed Bone Using Octacalcium Phosphate and Bone Matrix Gelatin in Rat Tibial Defects. Arch Bone Jt Surg. 2019 Mar; 7(2):182-190. Sargolzaei Aval F, Arab MR, Sargolzaei N, Barfrushan S, Mir M, Sargazi GH, Sargolzaeiaval F, Arab M. PMID: 31211197.
      View in: PubMed   Mentions: 1  
    4. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures. Mol Genet Genomic Med. 2018 11; 6(6):1148-1156. Sargolzaeiaval F, Zhang J, Schleit J, Lessel D, Kubisch C, Precioso DR, Sillence D, Hisama FM, Dorschner M, Martin GM, Oshima J. PMID: 30393977.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    5. Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients. Mol Syndromol. 2018 Jul; 9(4):214-218. Maezawa Y, Kato H, Takemoto M, Watanabe A, Koshizaka M, Ishikawa T, Sargolzaeiaval F, Kuzuya M, Wakabayashi H, Kusaka T, Yokote K, Oshima J. PMID: 30140198.
      View in: PubMed   Mentions: 2  
    6. Uncommon cause of cirrhosis-A case of Werner syndrome with a novel WRN mutation. Indian J Gastroenterol. 2017 Jul; 36(4):323-325. Amalnath SD, Sargolzaeiaval F, Oshima J, Baskar D. PMID: 28795391.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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