E-LIB Suche - Ergebnisse für: Poyrazoglu, Hatice Gamze

1

Broad-spectrum XX and XY gonadal dysgenesis in patients wit..:

Cicek, Dilek ; Warr, Nick ; Yesil, Gozde...
European Journal of Endocrinology. 186 (2022) 1 - p. 65-72 , 2022

Link: https://doi.org/10.1530/..

2

Clinical and molecular evaluation of MEFV gene variants in ..:

Yararbas, Kanay ; Yilmaz, Mustafa ; Tasdemir, Mehmet...
Functional & Integrative Genomics. , 2022

Link: https://hdl.handle.net/1..

3

Renal manifestations in children with neurofibromatosis typ..:

Celik, Binnaz ; Aksoy, Ozlem Yuksel ; Bastug, Funda.
European Journal of Pediatrics. 180 (2021) 12 - p. 3477-3482 , 2021

Link: https://doi.org/10.1007/..

4

Pelvic and breast ultrasound abnormalities and associated m..:

Aydin, Banu K. ; Kadioglu, Alev ; Kaya, Gamze A....
Clinical Endocrinology. 96 (2021) 3 - p. 339-345 , 2021

Link: https://doi.org/10.1111/..

5

A Rare Cause of Spasticity and Microcephaly: Argininemia:

Soylu Üstkoyuncu, Pembe ; Kendirci, Mustafa ; Gökay, Songül...
Turkish Journal Of Neurology. 26 (2020) 3 - p. 250-252 , 2020

Link: https://doi.org/10.4274/..

6

A Rare Cause of Spasticity and Microcephaly: Argininemia:

Pembe Soylu Üstkoyuncu ; Mustafa Kendirci ; Songül Gökay...
https://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-97752&look4=. , 2020

Link: https://doi.org/10.4274/..

7

Predictive value of laboratory parameters in childhood migr..:

Poyrazoğlu, Hatice Gamze ; Öztürk, Agah Bahadır
Acta Neurologica Belgica. 120 (2019) 4 - p. 907-914 , 2019

Link: https://doi.org/10.1007/..

8

Screening Inherited Metabolic Disorder in Children with Int..:

Soylu Üstkoyuncu, Pembe ; Güven, Ahmet Sami ; Poyrazoğlu, Hatice Gamze...
Turkish Journal Of Neurology. 25 (2019) 3 - p. 135-139 , 2019

Link: https://doi.org/10.4274/..

9

Screening Inherited Metabolic Disorder in Children with Int..:

Pembe Soylu Üstkoyuncu ; Ahmet Sami Güven ; Hatice Gamze Poyrazoğlu...
http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-82608&look4=. , 2019

Link: https://doi.org/10.4274/..

10

Body mass index at the presentation of premature adrenarche..:

Kaya, Gamze ; Yavas Abali, Zehra ; Bas, Firdevs..
European Journal of Pediatrics. 177 (2018) 11 - p. 1593-1601 , 2018

Link: https://doi.org/10.1007/..

11

L-2-hydroxyglutaric aciduria: Two cases:

Poyrazoglu, Hatıce Gamze ; Kara, Aslihan
European Journal of Paediatric Neurology. 21 (2017) - p. e134 , 2017

Link: https://doi.org/10.1016/..

12

Evaluation of carotid intima-media thickness in children wi..:

Poyrazoglu, Hatice Gamze ; Vurdem, Umit Erkan ; Arslan, Alev.
Neurological Sciences. 37 (2016) 10 - p. 1663-1669 , 2016

Link: https://doi.org/10.1007/..

13

Combination of two different homozygote mutations in Pompe ..:

Arslan, Alev ; Poyrazoğlu, Hatice Gamze ; Kiraz, Aslihan...
Pediatrics International. 58 (2016) 3 - p. 241-243 , 2016

Link: https://doi.org/10.1111/..

14

Tyrosinemia type II: Novel mutations in TAT in a boy with u..:

Gokay, Songul ; Kendirci, Mustafa ; Ustkoyuncu, Pembe Soylu...
Pediatrics International. 58 (2016) 10 - p. 1069-1072 , 2016

Link: https://doi.org/10.1111/..

15

Assessment of Psychopathology and Quality of Life in Childr..:

Öztop, Didem Behice ; Taşdelen, Bedia İnce ; PoyrazoğLu, Hatıce Gamze...
Journal of Child Neurology. 31 (2016) 7 - p. 837-842 , 2016

Link: https://doi.org/10.1177/..