Search Results - "Alzouman, Muneerah A."

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  1. 1
    Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans

    Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans by Shaheen, Ranad, Alsahli, Saud, Ewida, Nour, Alzahrani, Fatema, Shamseldin, Hanan E., Patel, Nisha, Al Qahtani, Awad, Alhebbi, Homoud, Alhashem, Amal, Al‐Sheddi, Tarfa, Alomar, Rana, Alobeid, Eman, Abouelhoda, Mohamed, Monies, Dorota, Al‐Hussaini, Abdulrahman, Alzouman, Muneerah A., Shagrani, Mohammad, Faqeih, Eissa, Alkuraya, Fowzan S.

    Published in Hepatology (Baltimore, Md.) (01-06-2020)
    “…Background and Aims The clinical consequences of defective primary cilium (ciliopathies) are characterized by marked phenotypic and genetic heterogeneity…”
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    Hereditary Leiomyomatosis and Renal Cell Carcinoma: A Case Report and Review of the Literature

    Hereditary Leiomyomatosis and Renal Cell Carcinoma: A Case Report and Review of the Literature by Alrawaf, Faisal A, Alamri, Eyad S, Al-Gonaim, Ali, Alzouman, Muneerah A, Alzahrani, Ahmed

    Published in Curēus (Palo Alto, CA) (29-10-2022)
    “…Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a rare genetic disorder, and individuals tend to develop multiple cutaneous leiomyomas, uterine…”
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  3. 3
    Hereditary Leiomyomatosis and Renal Cell Carcinoma: A Case Report and Review of the Literature

    Hereditary Leiomyomatosis and Renal Cell Carcinoma: A Case Report and Review of the Literature by Alrawaf, Faisal A, Alamri, Eyad S, Al-Gonaim, Ali, Alzouman, Muneerah A, Alzahrani, Ahmed

    Published in Cureus (01-10-2022)
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