Results 91 to 100 of about 1,360 (116)

A Rare Malignancy; Primary Peritoneal Serous Carcinoma in Men with ¹⁸F-FDG PET/CT and Histopathology. [PDF]

Mol Imaging Radionucl Ther
Özdemir Günay B, Günay B, Can N, Üstün F.   +3 more
europepmc   +1 more source

Pyomyositis as Presentation of Chemoport-related Infection in Breast Carcinoma: ¹⁸F-FDG PET/CT Findings. [PDF]

Mol Imaging Radionucl Ther
Singh V, Srivastava D, Kotarya N, Ora M, Gambhir S.   +4 more
europepmc   +1 more source

Short- and Long-Term Statin Persistence and Determinants in Patients Initiating Statin Therapy. [PDF]

Medeni Med J
Uzunlulu M, Torun C, Eken E, Ayasgil Ulas G, Castur L.   +4 more
europepmc   +1 more source

Factor deficiency in pregnancy and the role of the delta hemoglobin indices. [PDF]

Turk J Obstet Gynecol
İpek G, Tanaçan A, Altındiş Bal A, Yücel Yetişkin FD, Demet İ, Başaran E, Pekcan G, Şahin D.   +7 more
europepmc   +1 more source

Atypical Presentation of Metastatic Castrate-resistant Prostate Cancer in a Middle Aged African Male with Good Response to Radioligand Therapy. [PDF]

Mol Imaging Radionucl Ther
Evbuomwan O, Endres W, Tebeila T, Engelbrecht G.   +3 more
europepmc   +1 more source

Macular Telangiectasia Type 2: Long-Term Disease Progression and Management of Complications. [PDF]

Turk J Ophthalmol
Özbek M, Artunay Ö, Koçak R, Hoşver İ, Şimşek M.   +4 more
europepmc   +1 more source

A Case of VEXAS Syndrome Presenting with Unexplained Headache [PDF]

Turk J Haematol
Ataş Ü, Alhan FN, Beypınar D, Şahin S, Keşkek ŞÖ.   +4 more
europepmc   +1 more source

TAFRO Syndrome Without Pathology Supporting Castleman Disease: To Be Treated as Idiopathic Multicentric Castleman Disease-TAFRO or a Distinct Disease Entity? [PDF]

Turk J Haematol
Li SY, Gao YH, Dang Y, Zhang L, Li J.
europepmc   +1 more source

Diagnosis and Evaluation of Treatment Response in Relapsing Polychondritis Using ¹⁸F-FDG PET/CT. [PDF]

Mol Imaging Radionucl Ther
Civan C, Işık EG, Has Şimşek D, Altınkaynak M, Kuyumcu S.   +4 more
europepmc   +1 more source

Pi*M Palermo Mutation in Bronchiectasis due to Alpha-1 Antitrypsin Deficiency: A Rare Genetic Cause. [PDF]

Medeni Med J
Yildirimli B, Dogan C, Yilmaz Gulec E, Seven Yalcin G.   +3 more
europepmc   +1 more source