Unveiling the Respiratory Muscle Strength in Duchenne Muscular Dystrophy: The Impact of Nutrition and Thoracic Deformities, Beyond Spirometry

Autor: Mine Yuksel Kalyoncu, Yasemin Gokdemir, Cansu Yilmaz Yegit, Muruvvet Yanaz, Aynur Gulieva, Merve Selcuk, Şeyda Karabulut, Neval Metin Çakar, Pinar Ergenekon, Ela Erdem Eralp, Gülten Öztürk, Olcay Unver, Dilsad Turkdogan, Yavuz Sahbat, Ahmet Hamdi Akgülle, Fazilet Karakoç, Bulent Karadag

Publikováno v: Children, Vol 11, Iss 8, p 994 (2024)

Background/Objectives: Duchenne muscular dystrophy (DMD) is the most prevalent progressive muscular dystrophy, and the guidelines recommend the regular assessment of respiratory muscle function. This study aimed to assess the relationship between max

Externí odkaz: https://doaj.org/article/a689175f9ed349d083e006ce91435711

Evaluation of vincristine-induced peripheral neuropathy in children with cancer: Turkish validity and reliability study

Autor: Özdemir, Bilge, Gerçeker, Gülçin Özalp, Özdemir, Emine Zahide, Yildirim, Büşra Güliz, Ören, Hale, Yiş, Uluç, Günay, Çağatay, Thomas, Gülten ÖZTÜRK

Publikováno v: In Journal of Pediatric Nursing September-October 2023 72:185-190

Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study

Autor: Çağatay Günay, Duygu Aykol, Özlem Özsoy, Ece Sönmezler, Yaren Sena Hanci, Bülent Kara, Deniz Akkoyunlu Sünnetçi, Naci Cine, Adnan Deniz, Tolgahan Özer, Cemile Büşra Ölçülü, Özlem Yilmaz, Seda Kanmaz, Sanem Yilmaz, Hasan Tekgül, Nihal Yildiz, Elif Acar Arslan, Ali Cansu, Nihal Olgaç Dündar, Fatma Kusgoz, Elif Didinmez, Pınar Gençpinar, Tuğçe Aksu Uzunhan, Biray Ertürk, Alper Gezdirici, Akif Ayaz, Akgün Ölmez, Müge Ayanoğlu, Ayşe Tosun, Yasemin Topçu, Betül Kiliç, Kürşad Aydin, Ezgi Çağlar, Özlem Ersoy Kosvali, Çetin Okuyaz, Şeyda Besen, Leman Tekin Orgun, İlknur Erol, Deniz Yüksel, Abdullah Sezer, Ergin Atasoy, Ülkühan Toprak, Serdal Güngör, Bilge Ozgor, Meral Karadağ, Cengiz Dilber, Bahtiyar Şahinoğlu, Emek Uyur Yalçin, Nilüfer Eldes Hacifazlioglu, Ahmet Yaramiş, Pınar Edem, Hande Gezici Tekin, Ünsal Yilmaz, Aycan Ünalp, Sevim Turay, Didem Biçer, Gülen Gül Mert, İpek Dokurel Çetin, Serkan Kirik, Gülten Öztürk, Yasemin Karal, Aslıhan Sanri, Ayşe Aksoy, Muzaffer Polat, Nezir Özgün, Didem Soydemir, Gamze Sarikaya Uzan, Döndü Ülker Üstebay, Ayşen Gök, Mehmet Can Yeşilmen, Uluç Yiş, Gökhan Karakülah, Ahmet Bursali, Yavuz Oktay, Semra Hiz Kurul

Publikováno v: Neuropediatrics.

Background Although the underlying genetic causes of intellectual disability (ID) continue to be rapidly identified, the biological pathways and processes that could be targets for a potential molecular therapy are not yet known. This study aimed to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4841c2282b9a7b14fabbf904507e8a32
https://doi.org/10.1055/a-2034-8528

Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

Autor: Ünsal Yılmaz, Kıvılcım Gücüyener, Merve Yavuz, İbrahim Öncel, Mehmet Canpolat, Sema Saltık, Olcay Ünver, Ayşegül Neşe Çıtak Kurt, Ayşe Tosun, Sanem Yılmaz, Bilge Özgör, İlknur Erol, Ülkühan Öztoprak, Duygu Aykol Elitez, Meltem Çobanoğulları Direk, Muhittin Bodur, Serap Teber, Banu Anlar, Sema Saltik, Duygu Aykol, Edibe Pembegül Yıldız, Coşkun Yarar, Bülent Kara, Şenay Haspolat, Faruk İncecik, Gültekin Kutluk, Cengiz Dilber, Nihal Olgac Dundar, Hüseyin Tan, Ercan Demir, Büşra Daşlı Dursun, Tuğçe Damla Dilek, Dilşad Türkdoğan, Dilek Yalnızoğlu, Salih Akbaş, Ayten Güleç, Deniz Yılmaz, Müge Ayanoğlu, Seda Kanmaz, Serdal Güngör, Gülten Öztürk, Şeyda Beşen, Göknur Haliloğlu, Nazlı Balcan Karaca, Selcan Öztürk, Deniz Yüksel, Esra Gürkaş, Seçil Oktay, Hepsen Mine Serin, Meral Karadağ, İsmail Hakkı Akbeyaz, Uluç Yiş, Burçin Gönüllü Polat, Mehmet Sait Okan, Ömer Bektaş, Leman Tekin Orgun, Ceren Günbey, Hüseyin Per, Pembe Gültutan, Semra Büyükkorkmaz Öztürk, Erhan Aksoy, Gülcan Akyüz, Hasan Tekgül, Fulya Kürekçi, A. Semra Hız Kurul, Kürşat Bora Çarman, Defne Alikılıç, Özgür Duman, Mustafa Kömür, Miraç Yıldırım, Nurettin Alıcı, Hakan Gümüş, Muzaffer Polat, Bahadır Konuşkan, Olcay Güngör, Gülen Gül Mert, Selvinaz Edizer, Filiz Mıhçı, Sedef Terzioğlu Öztürk, Rabia Tütüncü Toker, Mutluay Arslan, Sevim Şahin, Pinar Gencpinar, Elif Yıldırım, Ersin Yüksel, Arzu Ekici, Adnan Deniz, Özlem Yayici Köken, Çetin Okuyaz, Nurşah Yeniay Süt, Ergin Atasoy, İsmail Solmaz, Mehmet Fatih Yetkin, Neslihan Bilgin, Aslı Kübra Atasever, Hande Gazeteci Tekin, İpek Dokurel, Aysima Özçelik, Ayşe Aksoy, Ayşe Nur Türköz, Dilek Cavusoglu, Mehbare Özkan, Emine Tekin, Türkan Uygur Şahin, Aycan Ünalp, Habibe Koç, Esra Sarıgeçili, Serdar Sarıtaş, Senem Ayça, Hülya Kayılıoğlu, Mine Çiğdem Şenoğlu, Tülay Kamaşak, Nargis Asadova, Filiz Keskin, Pakize Karaoğlu, Rojan İpek, Hamit Acer

Background: The discovery of anti-myelin oligodendrocyte glycoprotein (MOG)-IgG and anti-aquaporin 4 (AQP4)-IgG and the observation on certain patients previously diagnosed with multiple sclerosis (MS) actually have an antibody-mediated disease manda

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7189bb594b8e7e139069b7085c4d9385
https://avesis.deu.edu.tr/publication/details/e770a716-7c76-47b6-ae1a-6a20fb66ce13/oai

The outcome of two SMA cases treated with nusinersen at seven hours and at three days of life: the earliest ever

Autor: Olcay Ünver, Tolga Çelik, Aslı Memişoğlu, Esra Esim Büyükbayrak, Fatma Tülin Şimşek, Gülten Öztürk, Gökçe Eser, Evrim Karadağ Saygı, Yasemin Gökdemir, Berin Aktekin, Dilşad Türkdoğan, Haluk Topaloğlu

New molecular therapies are available for the treatment of spinal muscular atrophy (SMA) but early intervention is required. We report two cases that were diagnosed prenatally, where treatment with nusinersen was initiated within 7 h and three days r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1719fc0ad4ae2f5ffedd92dc390b4dc7
https://hdl.handle.net/11424/291026