JOURNAL OF PEDIATRIC NEUROLOGY
Official Journal of the World Pediatric Society, Turkiye
30th Annual Meeting of European Academy of Childhood Disability (EACD) will take place in Tbilisi, Georgia, May 28-31, 2018, https://www.eacd2018.net
LAST ISSUE
Rana, Abhilasha;Krishnan, Venkatram;Jamwal, Rupie:
Spinal Dysraphism Spectrum: A Novel Protocol-based Approach for Accurate Diagnosis on Imaging
Original Article
Gowda, Vykuntaraju K.;Channabasappa, Basavakumar;Shivappa, Sanjay K.;Veerappa, Basavaraja G.;Lakshmikantha, Keshavamurthy Mysore:
The Clinical, Laboratory, Etiological Profile and Outcome of Acute Necrotizing Encephalitis of Childhood (ANEC) in Tertiary Care Centre from Southern India
Cebeci, Hakan;Rykken, Jeffrey;Ott, Frederick;Folkertsma, Mark;Koksel, Yasemin;Gencturk, Mehmet:
Microstructural Changes in Normal-Appearing White Matter in Pediatric X-Linked Adrenoleukodystrophy: A Diffusion Tensor Imaging Study
Hassanein, Sahar M.A.;Elagouza, Iman;Sakr, Hossam;Mohammed, Maha Z.;Rihan, Ahmed;Deifalla, Shaymaa:
Diaphragmatic and Rectus Femoris Muscles Ultrasonography in Relation to Motor and Respiratory Functions in Ambulatory Boys with Duchenne Muscular Dystrophy
Case Report
Bastos, Paulo André Dias;Barbosa, Raquel:
A Newly Identified Int22h1/Int22h2‐Mediated Xq28 Duplication Syndrome Case Misdiagnosed as Cerebral Palsy
Shabo, Leah;Ishaque, Mariam;Sarathy, Danyas;Kumar, Jeyan;Xixis, Kathryn;Park, Min:
Pediatric Tacrolimus-Induced Reversible Cerebral Vasoconstriction Syndrome after Heart Transplantation
Samur, Bahadir M.;Ercan-Sencicek, Gulhan A.;Gumus, Hakan;Gumus, Gulsum;Baykan, Ali;Caglayan, Ahmet Okay;Per, Huseyin:
Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1
Das, Suman;Ray, Biman K.;Chakraborty, Uddalak;Kabiraj, Sujoy:
A Novel Variant of the Short-Chain Enoyl-CoA Hydratase-1 Gene Presenting with a Mild Phenotype: The Second Case Report from India
Freitas, Leonardo F.;Ribeiro, Lays S.;Duarte, Márcio L.;Silva, Mayara O. da;Ferreira, Paula M.:
Coffin–Siris Syndrome in a Patient with Hirschsprung's Disease—Expanding the Phenotype by Mutation ARID1B: A Case Report and Literature Review
Singh, Kushagra;Lohiya, Sham;Ganvir, Shubhangi;Damke, Sachin:
A Case of Acute Necrotizing Encephalitis Following Coronavirus Disease 2019 Infection—A Rare Presentation
Jain, Mukesh Kumar;Behera, Chinmaya Kumar;Panda, Sangram;Patnaik, Sibabratta;Sahoo, Bandya;Mishra, Reshmi;Behera, Jyoti Ranjan:
A Rare Case of Encephalopathy in Children—Known but Unknown
Yadav, Kusumlata;Mishra, Arpita;Narayan, Raghvendra;Singh, Ashok;Agrawal, Ritesh;Mishra, Om Prakash:
Homocystinuria Presenting as Ectopia Lentis and Thrombotic Manifestations in Two Siblings: A Case Series
Nagabushana, Divya;Samaga, Vishal Vishnuram;Shenoy, Sangeetha;Girishan, Shabari;V. Reddy, Hamsa;AR, Somashekhar:
Coronavirus Disease 2019-Associated Cerebral Mucormycosis in an Immunocompetent Child
Oyuela-Mancera, Martha E.;Maturana, Jennifer R.;Rodriguez, Laura C.;Perez-Acosta, Juan J.;Rodado-Mieles, César E.;Bastidas, Nicolás:
Thalamic Gangliocytoma in a Pediatric Patient—An Incidental Diagnosis
Letter to the Editor
Huddar, Akshata;Govindaraj, Periyasamy;Chiplunkar, Shwetha;Nagappa, Madhu;Taly, Arun B.;Sankaran, Bindu Parayil:
Paroxysmal Dystonia in a Child with Enoyl-CoA Hydratase Short-Chain 1 (ECHS1) Mutations
Erratum
Samur, Bahadir M.;Ercan-Sencicek, Gulhan A.;Gumus, Hakan;Gumus, Gulsum;Baykan, Ali;Caglayan, Ahmet Okay;Per, Huseyin:
Erratum: Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1