Søgeresultater - Dündar, Nihal

Comparison of the Efficacy and Safety of Insulin Glargine and Insulin Detemir with NPH Insulin in Children and Adolescents with Type 1 Diabetes Mellitus Receiving Intensive Insulin... af Dündar, Bumin Nuri, Dündar, Nihal, Eren, Erdal

Få fuldtekst Få fuldtekst Få fuldtekst

Adipokines in Breast Milk: An Update af Çatlı, Gönül, Olgaç Dündar, Nihal, Dündar, Bumin Nuri

Få fuldtekst Få fuldtekst Få fuldtekst

Electrical Status Epilepticus During Slow-wave Sleep (ESES): Current Perspectives af Arican, Pinar, Gencpinar, Pinar, Olgac Dundar, Nihal, Tekgul, Hasan

Få fuldtekst Få fuldtekst Få fuldtekst

Prevalence of Metabolic Syndrome in Obese Children and Adolescents using Three Different Criteria and Evaluation of Risk Factors af Sangun, Özlem, Dündar, Bumin, Köşker, Muhammet, Pirgon, Özgür, Dündar, Nihal

Få fuldtekst Få fuldtekst Få fuldtekst

Pregnancy Outcome after Varenicline Exposure in the First Trimester af Kaplan, Yusuf Cem, Olgac Dündar, Nihal, Kasap, Burcu, Karadas, Barıs

Få fuldtekst Få fuldtekst Få fuldtekst

Magnetic resonance imaging findings of two sisters with Van der Knaap leukoencephalopathy af Koç, Koray, Koç, Pınar, Karaali, Kamil, Olgaç Dündar, Nihal, Şenol, Utku, Canan, Arzu

Få fuldtekst Få fuldtekst Få fuldtekst

ITPA Related Developmental Encephalopathy: Key Role of Neuroimaging af Çavuşoğlu, Dilek, Kulali, Melike Ataseven, Dündar, Nihal Olgaç, Gokaslan, Cigdem Ozer, Aydin, Kurşad

Få fuldtekst Få fuldtekst Få fuldtekst

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism af Sangün, Özlem, Demirci, Serpil, Dündar, Nihal, Pirgon, Özgür, Koca, Tuğba, Doğan, Melike, Dündar, Bumin

Få fuldtekst Få fuldtekst Få fuldtekst

A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical Spectrum af Arican, Pinar, Cavusoglu, Dilek, Gencpinar, Pinar, Ozyilmaz, Berk, Ozdemir, Taha Resid, Dundar, Nihal Olgac

Få fuldtekst Få fuldtekst Få fuldtekst

Various Neurological Symptoms with Vitamin B12 Deficiency and Posttreatment Evaluation af Arıcan, Pinar, Bozkurt, Oznur, Cavusoglu, Dilek, Gencpınar, Pinar, Haspolat, Senay, Duman, Ozgur, Olgac Dundar, Nihal

Få fuldtekst Få fuldtekst Få fuldtekst

Interleukin-1β Secretion in Hippocampal Sclerosis Patients with Mesial Temporal Lobe Epilepsy af Dundar, Nihal Olgac, Aktekin, Berrin, Ekinci, Nilufer Cicek, Sahinturk, Duygu, Yavuzer, Ugur, Yegin, Olcay, Haspolat, Senay

Få fuldtekst Få fuldtekst Få fuldtekst

Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability af Arican, Pinar, Olgac Dundar, Nihal, Ozyilmaz, Berk, Cavusoglu, Dilek, Gencpinar, Pinar, Erdogan, Kadri Murat, Saka Guvenc, Merve

Få fuldtekst Få fuldtekst Få fuldtekst

Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development af AKSEL KILIÇARSLAN, Özge, ATAMAN, Esra, GÜRSOY, Semra, GÜRBÜZ, Gürkan, ÜNALP, Aycan, GENÇPINAR, Pınar, OLGAÇ DÜNDAR, Nihal, EDİZER, Selvinaz, ÜLGENALP, Ayfer, GİRAY BOZKAYA, Özlem

Få fuldtekst Få fuldtekst Få fuldtekst

Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy af Gursoy, Semra, Ataman, Esra, Baysal, Bahar Toklu, Özyılmaz, Berk, Gençpınar, Pınar, Hız, Ayşe Semra, Yiş, Uluç, Ünalp, Aycan, Dündar, Nihal Olgaç, Ülgenalp, Ayfer, Erçal, Derya

Få fuldtekst Få fuldtekst Få fuldtekst

Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia af Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Müller, Juliane S, Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M, Alfares, Ahmed A, Zhu, Changlian, Uhrova Meszarosova, Anna, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R, Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T, Strom, Tim M, De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P, Portier, Ruben, Bergmann, Carsten, Ghasemi Firouzabadi, Saghar, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A, Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W, Tran Mau-Them, Frederic, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laëtitia, Schmitt, Emmanuelle, Lacaze, Elodie, Küpper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J H, Grand, Katheryn, Graham, John M, Lewis, Richard A, Millan, Francisca, Duman, Özgür, Dündar, Nihal, Uyanik, Gökhan, Schöls, Ludger, Nürnberg, Peter, Nürnberg, Gudrun, Catala Bordes, Andrea, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Bouçanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S, Shamseldin, Hanan, Al Tala, Saeed, Rezazadeh Varaghchi, Jamileh, Najafi, Maryam, Deschner, Selina, Gläser, Dieter, Hüttel, Wolfgang, Kruer, Michael C, Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Züchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schüle, Rebecca, Horvath, Rita, Houlden, Henry, Bartesaghi, Luca, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark, Senderek, Jan

Få fuldtekst Få fuldtekst Få fuldtekst

Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia af Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Müller, Juliane S, Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M, Alfares, Ahmed A, Zhu, Changlian, Uhrova Meszarosova, Anna, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R, Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T, Strom, Tim M, De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P, Portier, Ruben, Bergmann, Carsten, Ghasemi Firouzabadi, Saghar, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A, Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair T, Wood, Nick W, Tran Mau-Them, Frederic, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laëtitia, Schmitt, Emmanuelle, Lacaze, Elodie, Küpper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J H, Grand, Katheryn, Graham, John M, Lewis, Richard A, Millan, Francisca, Duman, Özgür, Olgac Dundar, Nihal, Uyanik, Gökhan, Schöls, Ludger, Nürnberg, Peter, Nürnberg, Gudrun, Català-Bordes, Andrea, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Bouçanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S, Shamseldin, Hanan, Al Tala, Saeed, Rezazadeh Varaghchi, Jamileh, Najafi, Maryam, Deschner, Selina, Gläser, Dieter, Hüttel, Wolfgang, Kruer, Michael C, Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Züchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schüle, Rebecca, Horvath, Rita, Houlden, Henry, Bartesaghi, Luca, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark, Senderek, Jan

Få fuldtekst Få fuldtekst Få fuldtekst