Yayınlar & Eserler

Makaleler 12
Tümü (12)
SCI-E, SSCI, AHCI (9)
SCI-E, SSCI, AHCI, ESCI (12)
ESCI (3)
Scopus (12)
TRDizin (4)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 4

2. THE WHOLE 13 EXONS OF GNAS1 GENE AND THE GENES FOR HEREDITARY OSTEODISTROPHIAS(HO) IN SAGLIKER SYNDROME(SS). COMBINATION-COMPULSION OF HEREDITARY OSTEODISTROPHIAS AND CHRONIC KIDNEY DISEASES (CKD) ?

51st Congress of the European-Renal-Association(ERA)/European-Dialysis-and-Transplant-Association (EDTA), Amsterdam, Hollanda, 31 Mayıs - 03 Haziran 2014, cilt.29, ss.381, (Özet Bildiri) identifier

3. Cephalometric evaluation of the patients with Sagliker Syndrome: A preliminary report

44th ERA-EDTA Congress, Barcelona, İspanya, 22 - 24 Haziran 2007, cilt.22, ss.361, (Özet Bildiri) identifier

4. Nephrosclerosis of primary hypertension starts first in the left kidney and this sign could be called as Ergun sign.

21st Scientific Meeting of the International-Society-of-Hypertension/5th Asian-Pacific Congress of Hypertension/29th Annual Scientific Meeting of the Japanese-Society-of-Hypertension, Fukuoka, Japonya, 15 - 19 Ekim 2006, cilt.24, ss.340-341, (Özet Bildiri) identifier
Metrikler

Yayın

16

Yayın (WoS)

16

Yayın (Scopus)

12

Atıf (WoS)

68

H-İndeks (WoS)

5

Atıf (Scopus)

70

H-İndeks (Scopus)

5

Açık Erişim

1
BM Sürdürülebilir Kalkınma Amaçları