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Fadi W. Abdul-Karim

Researcher at Cleveland Clinic

Publications -  230
Citations -  8476

Fadi W. Abdul-Karim is an academic researcher from Cleveland Clinic. The author has contributed to research in topics: Cancer & Fine-needle aspiration. The author has an hindex of 49, co-authored 228 publications receiving 7974 citations. Previous affiliations of Fadi W. Abdul-Karim include University Hospitals of Cleveland & University of Texas at Austin.

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Positron Emission Tomography for Evaluating Para-aortic Nodal Metastasis in Locally Advanced Cervical Cancer Before Surgical Staging: A Surgicopathologic Study

TL;DR: Cervical cancers have a high avidity for FDG, and the use of PET-FDG scanning accurately predicts both the presence and absence of pelvic and para-aortic nodal metastatic disease.
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The meiotic competence of in-vitro matured human oocytes is influenced by donor age: evidence that folliculogenesis is compromised in the reproductively aged ovary.

TL;DR: It is postulate that an age- related decline in the process of folliculogenesis results in reduced oocyte quality and that the well characterized age-related increase in meiotic non-disjunction is one symptom of compromised oocyte growth.
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FOXA1 is an essential determinant of ERα expression and mammary ductal morphogenesis

TL;DR: Foxa1 deficiency causes a defect in hormone-induced mammary ductal invasion associated with a loss of terminal end bud formation and ERα expression, revealing that FOXA1 is necessary for hormonal responsiveness in the developing mammary gland and ER α-positive breast cancers, at least in part, through its control of ER α expression.
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Evidence of Independent Origin of Multiple Tumors From Patients With Prostate Cancer

TL;DR: The data suggest that multiple tumors in some patients with prostate cancer have independent origin, compared with either intraglandular dissemination or independent origin of prostate cancer.
Journal Article

Childhood fibrous tumor with psammoma bodies. Clinicopathologic features in two cases.

TL;DR: A fibrous tumor with psammomatous calcifications and lymphoplasmacytic cell infiltrate occurred in two children and could represent a distinctive lesion or late stages of calcifying aponeurotic fibroma, or inflammatory pseudotumor.