Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases

by Yiş, Uluç, Hız, Semra, Anal, Özden, Dirik, Eray
Published 2011

Obstructive hydrocephalus resulting from cerebral venous thrombosis

by Leblebisatan, Göksel, Yiş, Uluç, Doğan, Mustafa, Derundere, Ümit
Published 2011

Schwartz–Jampel syndrome with gastroduodenal bleeding

by Polat, İpek, Karaoğlu, Pakize, Yiş, Uluç, Kurul, Semra Hız
Published 2016

Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases

by Karaoğlu, Pakize, Polat, Ayşe İpek, Yiş, Uluç, Hız, Semra
Published 2015

A novel mutation in the sodium channel α1 subunit gene in a child with Dravet syndrome in Turkey☆

by Arslan, Mutluay, Yiş, Uluç, Çağlayan, Hande, Akin, Rıdvan
Published 2013

Coexistence of myositis, transverse myelitis, and Guillain Barré syndrome following Mycoplasma pneumoniae infection in an adolescent

by Topcu, Yasemin, Bayram, Erhan, Karaoglu, Pakize, Yis, Uluc, Guleryuz, Handan, Kurul, Semra Hiz
Published 2013

The combination of thermal dysregulation and agenesis of corpus callosum: Shapiro's or/and reverse Shapiro's syndrome

by Topcu, Yasemin, Bayram, Erhan, Karaoglu, Pakize, Yis, Uluc, Kurul, Semra Hiz
Published 2013

Kabuki syndrome and perisylvian cortical dysplasia in a Turkish girl

by Topcu, Yasemin, Bayram, Erhan, Karaoglu, Pakize, Yis, Uluc, Kurul, Semra Hız
Published 2013

Importance of acrocyanosis in delayed walking

by Yiş, Uluç, Polat, İpek, Karakaya, Pakize, Ayanoğlu, Müge, Hiz, Ayşe Semra
Published 2015

Importance of acylcarnitine profile analysis for disorders of lipid metabolism in adolescent patients with recurrent rhabdomyolysis: Report of two cases

by Topçu, Yasemin, Bayram, Erhan, Karaoğlu, Pakize, Yiş, Uluç, Kurul, Semra Hız
Published 2014

Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies

by Yis, Uluç, Baydan, Figen, Karakaya, Mert, Hız Kurul, Semra, Cirak, Sebahattin
Published 2016

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

by Rohrbach, Marianne, Vandersteen, Anthony, Yiş, Uluç, Serdaroglu, Gul, Ataman, Esra, Chopra, Maya, Garcia, Sixto, Jones, Kristi, Kariminejad, Ariana, Kraenzlin, Marius, Marcelis, Carlo, Baumgartner, Matthias, Giunta, Cecilia
Published 2011

Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

by Morimoto, Marie, Myung, Clara, Beirnes, Kimberly, Choi, Kunho, Asakura, Yumi, Bokenkamp, Arend, Bonneau, Dominique, Brugnara, Milena, Charrow, Joel, Colin, Estelle, Davis, Amira, Deschenes, Georges, Gentile, Mattia, Giordano, Mario, Gormley, Andrew K., Govender, Rajeshree, Joseph, Mark, Keller, Kory, Lerut, Evelyne, Levtchenko, Elena, Massella, Laura, Mayfield, Christy, Najafian, Behzad, Parham, David, Spranger, Jurgen, Stenzel, Peter, Yis, Uluc, Yu, Zhongxin, Zonana, Jonathan, Hendson, Glenda, Boerkoel, Cornelius F.
Published 2016