Makaleler
Tümü (26)
SCI-E, SSCI, AHCI (26)
SCI-E, SSCI, AHCI, ESCI (26)
Scopus (26)
2018
20181. Crizotinib Efficacy in ALK-Positive Advanced Stage Non-Small Cell Lung Cancer Patients: A Real-World Experience from Turkey
Kilickap S., Ozturk A., Karadurmus N., Korkmaz T., Yumuk P., Cicin I., et al.
JOURNAL OF THORACIC ONCOLOGY
, cilt.13, sa.10, 2018 (SCI-Expanded, Scopus)
2015
20152. GENERAL ASESSMENT OF UNLICENSED ANTINEOPLASTIC AND IMMUNOMODULATING MEDICINE USAGE IN TURKEY
Tuna E., Kockaya G., Yenilmez F. B., Dogan E., Vural I. M., Akbulat A., et al.
VALUE IN HEALTH
, cilt.18, sa.7, 2015 (SCI-Expanded, SSCI, Scopus)
2015
20153. GENERAL ASSESSMENT OF UNLICENSED MEDICINE USAGE IN TURKEY
Dogan E., Kockaya G., Tuna E., Yenilmez F. B., Vural I. M., Akbulat A., et al.
VALUE IN HEALTH
, cilt.18, sa.7, 2015 (SCI-Expanded, SSCI, Scopus)
2015
20154. GENERAL ASSESSMENT OF UNLICENSED ANTINEOPLASTIC AND IMMUNOMODULATING MEDICINE USAGE SUBGROUPS IN TURKEY
Yenilmez F. B., Kockaya G., Dogan E., Tuna E., Vural I. M., Akbulat A., et al.
VALUE IN HEALTH
, cilt.18, sa.7, 2015 (SCI-Expanded, SSCI, Scopus)
2012
20125. DIETARY MANAGEMENT AND GROWTH OF TETRAHYDROBIOPTERIN RESPONSIVE TURKISH PKU PATIENTS
Gokmen-Ozel H., Unal O., Kalkanoglu-Sivri H. S., Koksal G., DURSUN A., Tokatli A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
20126. MOLECULAR CHARACTERISATION OF BIOTINIDASE GENE MUTATIONS IN TURKISH PATIENTS; AN UPDATE OF THE RESULTS
Karaca M., Yucel D., Unal O., Guzel A., TOKATLI A., COŞKUN T., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
20127. ENZYME REPLACEMENT THERAPY (ERT)RESULTS OF PATIENTS WITH MUCOPOLYSACCHARIDOSIS TYPE II (HUNTER SYNDROME)
Unal O., Dogru-Ersoz D., Alehan D., Saglam M., Hismi B., DURSUN A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
20128. A PATIENT WITH PYRUVATE CARBOXYLASE DEFICIENCY AND NEMALINE RODS ON MUSCLE BIOPSY
Unal O., ÖZTÜRK HİŞMİ B., DURSUN A., Tokatli A., Coskun T., Wibrand F., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
20129. MOLYBDENUM COFACTOR (MOCO) DEFICIENCY TYPE B; CLINICAL, BIOCHEMICAL AND NEUROIMAGING FEATURES OF FIVE PATIENTS WTH TWO NOVEL MUTATIONS
ÖZTÜRK HİŞMİ B., Unal O., Sass J. O., Beermann F., Ichida K., DURSUN A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
201210. FEVER OF UNKNOWN ORIGIN IN A YOUNG ADULT WITH END-STAGE RENAL DISEASE, PREMATURE CORONARY ARTERY DISEASE AND POLYNEUROPATHY
ÖZTÜRK HİŞMİ B., Yasar Y., Unal O., Kilic L., Turkmen E., Erdem Y., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
201211. PROPIONIC ACIDEMIA PRESENTING WITH PERSISTENT PULMONARY HYPERTENSION IN TWO NEONATES
Hismi B., TEKŞAM Ö., Unal O., Takci S., Ertugrul İ., SİVRİ H. S., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
201212. SEVERE AZOTEMIA AND HYPERNATREMIC DEHYDRATION IN AN INFANT WITH PHENYLKETONURIA
Unal O., DÜZOVA A., ÖZTÜRK HİŞMİ B., DURSUN A., Tokatli A., Coskun T., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2012
201213. ACUTE INTERMITTENT PORPHYRIA: STILL UNCALLED BY PHYSICIANS
ÖZTÜRK HİŞMİ B., Tanriover M. D., Unal O., Sener E., TEMUÇİN Ç. M., Sivri H. S., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.35, 2012 (SCI-Expanded, Scopus)
2011
201114. ACUTE RESPIRATORY DISTRESS SYNDROME IN TWO PATIENTS WITH ORGANIC ACIDEMIA INVOLVING PROPIONATE METABOLISM
Unal O., ÖZTÜRK HİŞMİ B., Sivri K. H. S., Dursan A., Tokatli A., Coskun T.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.34, 2011 (SCI-Expanded, Scopus)
2011
201115. CHALLENGES IN THE TREATMENT OF A PATIENT AFFECTED BY BOTH ARGININOSUCCINIC ACIDURIA AND METHYLMALONIC ACIDURIA
Unal O., ÖZTÜRK HİŞMİ B., Coskun T., Tokatli A., DURSUN A., Sivri K. H. S.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.34, 2011 (SCI-Expanded, Scopus)
2011
201116. HEMOPHAGOCYTOSIS IN THREE PATIENTS WITH ORGANIC ACIDEMIA INVOLVING PROPIONATE METABOLISM
Gokce M., Unal O., ÖZTÜRK HİŞMİ B., Gumruk F., Coskun T., DURSUN A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.34, 2011 (SCI-Expanded, Scopus)
2010
201017. MUTATION PROFILE OF BCKDHA, BCKDHB AND DBT GENES FOR MAPLE SYRUP URINE DISEASE IN TURKEY
Ozgul R. K., Guzel A., Dundar H., Yucel D., Yilmaz A., Unal O., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.33, 2010 (SCI-Expanded, Scopus)
2010
201018. SIX NOVEL MUTATIONS IN TURKISH PATIENTS WITH ISOVALERIC ACIDEMIA
Kucuk O., Ozgul R. K., Karaca M., Sivri H. S., Coskun T., Tokatli A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.33, 2010 (SCI-Expanded, Scopus)
2010
201019. THE SPECTRUM AND FREQUENCY OF ALDOLASE B GENE MUTATIONS IN TURKISH PATIENTS WITH HEREDITARY FRUCTOSE INTOLERANCE
Yucel D., Ozgul R. K., Yilmaz A., Sivri H. S., Coskun T., Unal O., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.33, 2010 (SCI-Expanded, Scopus)
2010
201020. A NOVEL MUTATION IN BETA KETOTHIOLASE DEFICIENCY
Unal O., ÖZTÜRK HİŞMİ B., Kilic M., DURSUN A., Kalkanoglu-Sivri H. S., Tokatli A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.33, 2010 (SCI-Expanded, Scopus)
2010
201021. MOLECULAR AND STRUCTURAL ANALYSIS OF SIX NONSENSE MUTATIONS IN MUT METHYLMALONIC ACIDEMIA PATIENTS INCLUDING TWO NOVEL NONSENSE MUTATIONS
Dundar H., Ozgul R. K., Unal O., Karaca M., Aydin H., Tokatli A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.33, 2010 (SCI-Expanded, Scopus)
2010
201022. POLYNEUROPATHY AS THE MAIN PRESENTING SYMPTOM IN PDH DEFICIENCY
Unal O., ÖZTÜRK HİŞMİ B., Kilie M., DURSUN A., Kalkanoglu-Sivri H. S., Tokatli A., et al.
JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.33, 2010 (SCI-Expanded, Scopus)
2009
200923. Efficacy of nasopharyngeal culture in identification of pathogen in middle ear fluid in chronic otitis media with effusion.
Eser Ö., Ipci K., Alp Ş., Akyol U., Unal O. F., Hascelik G., et al.
Indian journal of medical microbiology
, cilt.27, ss.237-41, 2009 (SCI-Expanded, Scopus)
2005
200524. Non-Hodgkin's lymphoma among the gamut of differential diagnoses for shoulder pain
Guven G., Solak Y., Unal O., Ozcakar L.
RHEUMATOLOGY INTERNATIONAL
, cilt.25, sa.7, ss.565-566, 2005 (SCI-Expanded, Scopus)
2004
200425. Magnetic resonance imaging: a sine qua non in the diagnosis of brucella spondylitis
Unal O., Ozcakar L., Inanici F.
CLINICAL RHEUMATOLOGY
, cilt.23, sa.5, ss.473-474, 2004 (SCI-Expanded, Scopus)
2003
200326. Severe Bilateral Carpal Tunnel Syndrome in Juvenile Chronic Arthritis
Unal O., Ozcakar L., Cetin A., Kaymak B.
Pediatric Neurology
, cilt.29, sa.4, ss.345-348, 2003 (SCI-Expanded, Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2014
20141. Early laboratory diagnosis and bone marrow transplantation in MPS type I
El Moustafa K., LAY İ., Unal O., Sivri S., Coskun T.
FEBS EMBO 2014 Conference, Paris, Fransa, 30 Ağustos - 04 Eylül 2014, cilt.281, ss.557-558, (Özet Bildiri)
2003
20032. Magnetic resonance imaging: A sine qua non in the diagnosis of brucella spondylitis
Unal O., Ozcakar L., Ynanycy F.
Annual European Congress of Rheumatology, Lisbon, Portekiz, 18 Haziran 2003, cilt.62, ss.517-518, (Özet Bildiri)