Cerebral Palsy and Neurodisability
Prevention and Cure of the Intrathecal Baclofen Pump . | |
Yasser Awaad |
Synergetic effect of intrathecal baclofen and deep brain stimulation in treating dystonia | |
Yasser Awaad |
Functional Assessment Following Intrathecal Baclofen Therapy in Children with Spastic Cerebral Palsy | |
Yasser Awaad |
Botulinum toxin- A in postoperative pediatric stiff hips | |
Yasser Awaad |
Frequency and predictive factors of scoliosis in Malaysian children with Cerebral Palsy | |
POORANI ANANDAKRISHNAN, TEIK BENG KHOO |
Cognitive profile in children with bilateral spastic cerebral palsy due to periventricular leukomalacia | |
Kaeko Ogura, Yukihiro Kitai, Satori Hirai, Hiroshi Arai |
Influence of plantar flexors spasticity on center of mass during walking among children with unilateral spastic cerebral palsy | |
Ehab Anwar Waly, Mai Ahmed |
Genomic analysis identifies pathogenic variants in 9 of 17 cases with full-term cerebral palsy | |
Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata-Uematsu, Takehiko Inui, Saeko Yamamura-Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki-Muromoto, Yukimune Okubo, Wakaba Endo, Noriko Togashi, Yasuko Kobayashi, Akira Onuma, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Yoko Aoki, Shigeo Kure |
Association of comorbidities in cerebral palsy with GMFCS, CP type and Quality of life : An observational study at a tertiary care hospital | |
JAYANTI PRABHA, areesha alam, Rashmi Kumar, Chandrakanta kumar, neera kohli |
Association of interleukin -6 Polymorphism and mRNA expression in cerebral palsy – a Pilot study | |
Anju Aggarwal, Sonali Verma, Anurupa Chakraborty, Neha Bansal, Shambhavi Roy |
Clinical course and seizure outcome of symptomatic epilepsy in cerebral palsy patients : community based study | |
Noha El tantawi, Dina Abd Elmegid |
Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET), Central Motor Conduction Times (CMCT) and Somatosensory Evoked Potentials (SEP) in children with dystonic cerebral palsy (CP) | |
Stavros Tsagkaris, Verity McClelland, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Alexander Hammers, Jean-Pierre Lin |
From cerebral palsy to hereditary spastic paraplegia: à propos of three patients | |
Dina Rose Amrom, Sara Seneca, Cedric Ballez, Monique Cordonnier, Peter De Jonghe, Jonathan Baets, Massimo Pandolfo, Julie Soblet, Guillaume Smits |
Clinical, radiological and genetic findings in a cohort of 60 polymicrogyria patients | |
Dina Rose Amrom, Annapurna Poduri, Nicolas Deconinck, Bernard Dan, Cynthia Prigogine, Anne Monier, Alec Aeby, Guillaume Smits, Emmanuel Scalais, Ingrid Unterberger, Eugen Trinka, François Dubeau, Donatella Tampieri, Jean-Claude Décarie, Jacques Michaud, Paul Mark, William B Dobyns, Christopher A Walsch, Frederick Andermann, Eva Andermann |
Mothers’ perception in changes of hand skills pattern of their children with cerebral palsy to perform activities of daily living in Bangladesh | |
Md. Yeasir Arafat Alve |
CNS Infections
Neurodevelopment of 24 children born in Brazil with congenital Zika syndrome in 2015 - case series study | |
Lucas Victor Alves, Camila E Parede, Germanna V Silva, Maria Julia Gonçalves Mello, João Guilherme Bezerra Alves |
Congenital Zika syndrome and infatile spasms - case series study | |
Lucas Victor Alves, Maria Júlia Gonçalves Mello, Patrícia Bezerra, João Guilherme Bezerra Alves |
Chikungunya infection and Horner Syndrome: a case report | |
Lucas Victor Alves, Filipe Marinho Pinheiro Câmara, Mayara Batista Granhara, Alfredo Meneses Neto, João Guilherme Bezerra Alves |
Differentiating Scrub typhus meningoencephalitis from other Acute Encephalitis Syndrome In children in Uttar Pradesh, India | |
Pranshi Agarwal, Areesha Alam, Jayanti Prabha, Amita Jain, Chandrakanta Kumar, Sanjeev Kumar Verma, Rashmi Kumar |
SUBACUTE SCLEROSING PANENCEPHALITIS IN POST-MEASLES VACCINATION ERA-THE CHANGING EPIDEMIOLOGICAL TRENDS AND NEED FOR EARLY VACCINATION | |
EKTA AGARWAL, Dr. Kavita Srivastav, Dr. Surekha Rajadhyaksha |
Congenital CMV infection- A rare cause of Central Diabetes Insipidus | |
Ambrin Akhtar |
Treatment outcome of children with Congenital CMV infection at ICH and Dr. MR Khan Shishu(Children) Hospital | |
MASHAYA ZAMAN KOLI, SELINA HUSNA BANU, RAWNAK ARA |
Clinico-epidemiological profile and outcome of pediatric neurotuberculosis: a retrospective cohort study | |
Biswaroop Chakrabarty, Vivek Sirolia, Mudit Aggarwal, Prashant Jauhari, Atin Kumar, Sheffali Gulati |
High burden of neurological presentations in children admitted to Kenyan hospitals: A multi-hospital cohort study. | |
Jane Hassell, Thomas Julius, Morris Ogero, Charles RJC Newton, Mike English, Sam Akech |
Education and Training
Flipped classroom versus traditional lecture in training undergraduate medical students on pediatric epilepsy: A randomized controlled trial | |
Jaya Shankar Kaushik, Vandana Arya, Radhamohan Rana, Anjali Verma, Harish Bhardwaj |
Development Cognition and Psychiatry
Predictors of intellectual abilities among children with autism spectrum disorder | |
Watfa Al-Mamari, Ahmed Babiker Idris, Ahlam Ali Abdelsattar, Abeer Al-Mujaini, Muna Al-Jabri |
A STUDY ON HEAVY METALS PROFILE IN CHILDREN WITH AUTISM | |
Mogili Sudha Priyanka, SAVITA VERMA ATTRI, PRATIBHA SINGHI, PRAHBHJOT MALHI, JITENDRA KUMAR SAHU, ARUSHI GAHLOT SAINI |
“Prevalence of Autism spectrum disorders (ASD) in a latinamerican city, first epidemilogical study in children 18 – 36 months of age” | |
Francisco Alberto Astorino, Elena Carrera, Liliana Contini |
Neurodevelopmental Outcome After Neonatal Hypoglycemic Brain Injury . | |
Madhavi Shelke, Abhay Jain, Madhura Anvikar, Pratima weldode, Abdul Muqueet |
Vitamin B12 status and Neurodevelopmental delay in Infants in Northern India | |
Chandrika Azad |
Comparison of Executive Function between children with Autism Spectrum Disorder and Typically Developing Children: a Cross-sectional study | |
Ratna Sharma, Asfa Ahmad, Shobha Sharma, Prateek Kumar Panda, Aparajita Gupta, Rupesh Samanchi, Sana Sayeed, Prashant Jauhari, Biswaroop Chakrabarty, Sheffali Gulati |
NON PHARMACOLOGICAL PROTOCOL FOR TREATING ADHD CHILDREN (NFB,CES,CCT) | |
hussein hosny abdeldayem |
The effect of omitting breakfast on cognitive function and blood glucose level among adolescent secondary school students | |
Halima Adamu |
Targeted gene sequencing in children with autism spectrum disorder | |
Mary Iype, Anitha Ayyappan, PA SURESH |
Shared atypical functional connectivity in children with autism spectrum disorder and attention- deficit/hyperactivity disorder | |
EVDOKIA ANAGNOSTOU |
A Phase 2 Randomized, Placebo-Controlled Trial of Tideglusib, an Orally Administered GSK3Beta Inhibitor, in the Treatment of Adolescents with Autism Spectrum Disorder | |
EVDOKIA ANAGNOSTOU |
Epilepsy
First Complex Febrile Seizure – do we need to investigate. | |
Arpita Devbrata Adhikari, Krishna Shetye, Smita Patil, Mona Gajre |
Prevalence of Epilepsy and Inter-ictal Epileptiform discharges in children with Neurodevelopmental disorders | |
B Anukirthiga, Devendra Mishra, Sanjay Pandey, Monica Juneja |
Seizures in children with Zika Virus Congenital Syndrome | |
Lucas Victor Alves, Patrícia Gomes de Matos Bezerra, Maria Júlia Gonçalves de Mello, Ana Rodrigues Falbo, José Natal Figueiroa |
A critical analysis of lumbar puncture in the emergency management of febrile seizures: a cross-sectional study | |
Eduardo Jorge da Fonseca Lima, Gabriel Brito de Moura Monteiro, Alberto de Barros Lima Filho, Lucas Victor Alves |
Ohtahara Syndrome due to unique Heterozygous PIGO mutation: Clinical and EEG features | |
Arayamparambil C Anilkumar |
National Surveillance of Mortality in Children with Epilepsy in the UK and Ireland | |
Omar Abdel-mannan, Alastair Sutcliffe |
Pediatric status epilepticus. Cases admitted during years 2015-2016 at Hospital de niños Dr. O. Alassia de la ciudad de Santa Fe, Argentina. | |
Francisco Alberto Astorino, Betiana Comas, María Inés Malatini |
Evolution of epileptic zeisures iniciated during neonatal period in a long term follow up of 97 children | |
Francisco Alberto Astorino, María Ines Malatini, Betiana Comas |
Febril status epilepticus in children. Series of cases of children admited at Dr. O Alassia Hospital, Santa Fe Argentina period 2015 to 2018 | |
Francisco Alberto Astorino, Betiana Comas, María Inés Malatini |
Autoimmunity of childhood epilepsy | |
sonali verma, Anju Aggarwal, Gargi Rai, Shukla Das |
Comparison Of Electroencephalographic Sleep Stages With Bispectral İndex Data İn Children | |
Sanem Yılmaz, Hasan Tekgul, Erdem Simsek, Hande Tekin, Hepsen Mine SERIN, Gul Aktan, Sarenur Gokben |
Comparison of Epileptic Seizure Classifications (ILAE-1981 and ILAE-2017) with A Modular Education Program Among Residents in Pediatrics | |
Meherrem Imanli, Hasan Tekgul, Erdem Simsek, Hepsen Mine Serin, Seda Kanmaz, Sanem Yilmaz, Gul Aktan, Sarenur Gokben |
Clinical profile and short-term outcome of status epilepticus in children | |
Chinmay Chetan, Satinder Aneja, Suvasini Sharma, Bijoy Patra, Surendra Bahadur Mathur |
SYNDROMES AND ETIOLOGY IN PEDIATRIC EPILEPSY: EVALUATION OF INTERNATIONAL LEAGUE AGAINST EPILEPSY (ILAE) 1989, 2010 AND 2017 CLASSIFICATION OF EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA | |
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, satinder aneja |
DESCRIPTIVE EPIDEMIOLOGY OF “CONTINUOUS SPIKE AND SLOW WAVE IN SLEEP (CSWS)” EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA | |
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, Satinder Aneja |
ELECTROCLINICAL PROFILES OF CHILDREN WITH BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES (BECTS) AT A TERTIARY CARE CENTRE | |
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, Satinder Aneja |
Infantile epilepsy with prolonged focal myoclonic seizures: A distinctive syndrome associated with TBC1D24 mutation. | |
Deepa Sirsi, John Schreiber, Satish Agadi, Robert S Greenwood, Susan T Arnold |
Outcome of Rasmussen Encephalitis with conservative management | |
Bijoy Patra, Surendra Bahadur Mathur, Kanti Lal Chakraborti, Preeti Gaddad, Suvasini Sharma, Satinder Aneja |
Prevalence and association of risk factors for anticonvulsant polytherapy amongst epileptic children: A case-control study | |
Shifa Bidhan, Krishna M Adhikari, Rakesh Kumar Gupta |
Clinical utility of next generation sequencing in Early-Onset Epileptic Encephalopathies | |
Vishal Sondhi, K M Adhikari, Vishal Vishnu Tewari, K Venkatnarayan, Rakesh Gupta |
Hypothyroidism and valproate: Is there a causal relationship? | |
Chhitiz Anand |
Epilepsy Versus Chronic diseases: How different are parent’s attitudes? | |
Noha El tantawi, Dina Abd Elmegid, Eman Atef |
Electrophysiological characteristics in children with Subacute sclerosing panencephalitis (SSPE): A study from a tertiary care hospital. | |
ANSHITA ARORA, SHILPA KULKARNI, MEENAL GARG, SONAM KOTHARI, ANAITA HEGDE, KRISHANKUMAR SHAH |
Does Ethnicity Affect the Clinical Presentation of Tuberous Sclerosis Complex? | |
Ravi Benjamin Dhamija, Cigdem Akman, Aliza Alter, Daniel McBrian, Elena Gonzalez |
Semiological, Diagnostic and theraupetic challenges in Infantile onset epilepsy | |
Smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Shah, Srikanth Domala, Prasanthi Aripirala, Ravi verma |
Retrospective cohort of Dravet syndrome due to SCN gene mutation from Southern India | |
Hemadriben Muljibhai Vegda, Vykuntaraju Gowda, Raghavendraswami Amoghimath, Asha benakappa |
Evolution of electroencephalogram findings in pontocerebellar hypoplasia type 2A | |
Rony Cohen, Yoram Nevo, Sara Kivity, Ayelet Halevy, Sharon Aharoni, Rachel Straussberg |
Verbal Semantics and Social cognition in adolescents with drug resistant refractory epilepsy | |
Sujit Abajirao Jagtap, SONAL CHITNIS, KINJAL JAIN, ANKIT ARORA, MEDHA ADHYRU, SANDEEP PATIL, NILESH KURWALE |
Assessment of quality of life in Omani children with epilepsy attending Sulatan Qaboos University Hospital | |
Amna Mohamed Al Futaisi |
Epilepsy in Children- Psychosocial and Emotional Impact on Their Siblings and Their Coping Skills | |
EKTA AGARWAL, Dr. Kavita Srivastav, Dr. Surekha Rajadhyaksha, Dr. Manjiri Datar |
Epidemiological Survey (three staged) of Pediatric Epilepsy in a rural suburb of Pune District | |
EKTA AGARWAL, Dr. Surekha Rajadhyaksha, Dr. Kavita Srivastav |
Asymptomatic malaria parasitaemia and seizure control in children with nodding syndrome; a cross sectional study | |
Rodney Ogwang, Ronald Anguzu, Pamela Akun, Albert Ningwa, Edward Kayongo, Kevin Marsh, Charles Newton, Richard Idro |
Neonatal-onset epilepsy: Clinico-etiological spectrum and short-term outcome | |
Prasanthi Aripirala, Ramesh Konanki, Lokesh Lingappa |
Headache
Examination of children with migraine; Three years experience | |
Deniz Karakaya, Deniz Yüksel, Hülya Kayılıoglu, Ayşe Aksoy, Ulkuhan Oztoprak, Çigdem Genç Sel, Erhan Aksoy, Ozge Dedeoglu |
Metabolic Disorders
DIAGNOSIS OF GM2 GANGLIOSIDOSIS WITH A NEW MUTATION | |
Rashmi Adiga, Neha Rajkumar Jain, Sudhindra Kulkarni, Kruti Varshney |
Hypocalcemia as a cause of breath holding spells in children below 6 months | |
Simran Jain, Neha Ahuja, Gouri Rao Passi |
An unusual presentation of Menkes disease masquerading as a leukodystrophy with macrocephaly | |
Aswini Annadurai, Anshula Tayal, Aman Elwadhi, Suvasini Sharma, Bijoy Patra |
Assessment of Vitamin B-12 deficiency and Risk Factors in Healthy Infants: A Cross-sectional Study | |
Kuchana Suresh Kumar, Savita Attri, Arushi Gahlot Saini, Bhavneet Bharti, Naveen Sankhyan, Prateek Bhatia, Ajay Patial |
GLUTARIC ACIDURIA TYPE 1: AN USUAL IMAGING FEATURE | |
SHRUTI HARSHAL AGRAWAL, SANGEETA RAVAT, VIRAJ SANGHI |
Spectrum of Inherited White Matter Disorders in Children and their Outcomes | |
Vijay Gonda, Arushi Gahlot Saini, Naveen Sankhyan, Jitendra Sahu, sameer vyas, Savita Attri, Inusha panigrahi |
A proposed staging system for CLN3 disease (Juvenile Batten Disease) | |
Jonathan W Mink, Justin Williams, Erika Augustine |
Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET) imaging and motor and sensory neurophysiology in children with Glutaric Aciduria(GA1) dystonia awaiting Deep Brain Stimulation Surgery (DBS) | |
Stavros Tsagkaris, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Verity McClelland, Alexander Hammers, Jean-Pierre Lin |
Movement Disorders
A novel frameshift mutation in SLC2A1 (GLUT1) associated with a mild form of carbohydrate-responsive movement disorder | |
Yasser Awaad |
A Rare Case Of Early Onset Hereditary spastic paraplegia caused by AFG3L2 and SPG7 mutations | |
Piyush Kumar Anshu, Dr Viraj Sanghi |
Clinical clues in etiological diagnosis of childhood ataxia | |
EKTA AGARWAL |
Muscle and Nerve
Incidence of infantile spinal muscular atrophy in Shikoku Island of Japan | |
Kentaro Okamoto, Mitsumasa Fukuda, Isao Saito, Risako Urate, Satoshi Maniwa, Daisuke Usui, Takahiro Motoki, Toshihiro Jogamoto, Kaori Aibara, Takatoshi Hosokawa, Yukihiko Konishi, Reiko Arakawa, Kenji Mori, Eiichi Ishii, Kayoko Saito, Hisahide Nishio |
Childhood Onset Limb Girdle Muscular Dystrophies in Aegean Part of Turkey | |
Uluç Yiş, Gülden Diniz, Filiz Hazan, hülya sevcan daimagüler, bahar toklu baysal, figen baydan, gülçin akıncı, aycan ünalp, gül aktan, erhan bayram, semra hız, cem paketçi, derya okur, erdener özer, ayça ersen danyeli, gökhan uyanık, sebahattin çırak |
Spinal Muscular Atrophy – Lower Extremity Dominant Type 2 (SMALED2) | |
Erdem Simsek, Sanem Yilmaz, Hepsen Mine SERIN, Seda Kanmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben |
UK initiative to speed up diagnosis of Duchenne muscular dystrophy worldwide | |
Henriette van Ruiten, Mayhew Anna, Helen Aspey, Robert Muni Lofra, Volker Straub, Michela Guglieri |
Pain prevalence and characteristics in spinal muscular atrophy type II | |
Yuu Uchio, Mikiko Hasegawa, Kouta Kajima, Hayato Suzuki, Kaho Nakamura, Midori Saito, Tetsuo Ikai, Futoshi Wada, Kayoko Saito, Reiko Arakawa, Osamu Nitta |
Bone Health Monitoring In Boys With Duchenne Muscular Dystrophy: A Survey Of Clinical Practice In The United Kingdom NorthStar Clinical Network | |
Shuko Joseph, Nadia Capaldi, Marina DiMarco, Iain A Horrocks, Volker Straub, S Faisal Ahmed, Michela Guglieri, Sze Choong Wong, North Star Clinical Network |
Guillain-Barre Syndrome: Uncommon association to common pediatric diseases | |
Marwa Abd Elmaksoud, Yasmine El Chazli, Shaymaa Elsayed |
Multiplex ligation-dependent probe amplification based SMN1 deletion analysis in 150-Indian patients with spinal muscular atrophy | |
Hansashree Padmanabha, Veeramani Preethish-Kumar, KIRAN POLAVARAPU, Saraswati Nashi, Seena Vengalil, Deepha Sekar, Nalini Atchyaram, Priya Thomas, KRISHNA GK |
EARLY CLINIC-ELCTROPHYSIOLOGICAL PREDICTORS OF POOR FUNCTIONAL OUTCOMEIN GBS | |
EKTA AGARWAL |
Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy | |
Ranjith Kumar Manokaran, Biswaroop Chakrabarty, Prashant Jauhari, Rakesh Kumar, Sandeep Aggarwala, Arun Gupta, Manisha Jana, R M Pandey, Sheffali Gulati |
Genetic evaluation of Congenital Myopathy (CM) and Congenital Muscular Dystrophy (CMD) in children : Slow Death of Muscle biopsies | |
RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, PRASHANTHI ARIPRALA, RAMPRASAD VL, THENRAL SG |
Clinicopathological profile and treatment outcome of Inflammatory myopathies in children: a retrospective cohort study | |
Prateek Kumar Panda, Vyshakh Anand, Prabhjoth Kaur, Prashant Jauhari, Biswaroop Chakrabarty, Atin Kumar, Manisha Jana, M C Sharma, Vaishali Suri, Chitra Sarkar, Sheffali Gulati |
Neonatal and Fetal Neurology
Description of primary neurologic phenotypes in congenital CMV infection | |
Hitha Vishwanath Amin, Lisa Emrick, Gail Demmler-Harrison |
Neurogenetics
Optic Atrophy and Retinal Pigmentary Changes: Expanding The Phenotypic Spectrum of Farber Lipogranulomatosis | |
Abdullah Saeed Alamri, Ali A AlFaiz, Daniah Alshowaeir, Fatimah Al Mousawi, Adel A Mahmoud, Aqeela Al-Hashim |
The Landscape of Genetic causes of basal ganglia and thalamus involvement in children based on the first 5000 MRI studies | |
SAAD ALSHAHWAN |
ISCA2 Related Mitochondrial Disorder: A distinct cause of Infantile Leucodystrophy | |
Sadia Tabassum, Rowim Al Mutairi, Mohammed Al Mannai, Ali Al Otaibi |
NDUFS6 mutations cause lethal neonatal mitochondrial complex I deficiency | |
MOHAMED ALJABRI |
Mutation Screening using Next Generation Sequencing (NGS) Gene Panel in Patients with Normal Targeted Metabolic Profiling | |
MAJED J. Dasouki, Amal Jabr, Ghadah AlDakheel, Mohamed Abouelhoda, Shazia Subhani, Fahd Elbadoui, Nada AlTassan, Dorota Monies |
Next generation sequencing: a magic bullet or a cautious sword? | |
Shruti Bajaj, Mamta Muranjan, Anaita Hegde, Mukesh Agrawal |
HECW2 mutation causes periodic attacks of paralysis, intellectual disability and hypotonia | |
Kazuyuki Nakamura, Takahiro Abiko, Takashi Kanbayashi, Mitsuko Nakashima, Hirotomo Saitsu, Naomichi Matsumoto, Mitsuhiro Kato |
A RARE TYPE OF HEREDITARY SENSORY AUTONOMIC NEUROPATHY | |
PRIYANKA SUNIL WALZADE, SHRUTI AGRAWAL, MANSI SHAH, VIRAJ SANGHI, SANGEETA RAVAT |
Gestalt Diagnosis of Children with Intellectual disability with Dysmorphism- Necessity for Establishing Genetic Diagnostic Approach. | |
Shaoli Sarker, Mustafa Mahbub, Narayan Saha, AZM AZAM, Humaira Rafiqa Quaderi, Shayla Imam Kanta, Sultana Razia, Fayaza Ahmed, Asma Hoque, Ahmed Asif Ferdous, Naila Zaman Khan |
Assessment of cardiac involvement in childhood Neurofibromatosis Type 1 diagnoses, identification of Rasopathic cases | |
Ilyas Emre Tekdemir, Deniz Yüksel, Vehbi Dogan, Ayşe Aksoy, Hulya Kayılıoglu, Ulkuhan Oztoprak, Erhan Aksoy, Cigdem Sel |
Clinical and Genetic Spectrum of Disorders with Cerebellar Atrophy | |
Ramya Bandi, lokesh lingappa, Prasanthi Aripirala, Rini Kothari, Ramesh Konanki, Nikit Milind Shah, Smilu Mohanlal, Thenral SG, Ramprasad VL |
“STUDY OF CLINICO-ETIOLOGICAL PROFILE OF EARLY ONSET EPILEPTIC ENCEPHALOPATHY IN CHILDREN’’ | |
Boda Praful Kumar, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, RADHA RAMA DEVI, PRASHANTHI ARIPIRALA, THENRAL SG |
Whole Exome Sequencing (WES) identifies PGAP3 mutation in three patients from two Saudi families with hyperphosphatasia with mental retardation syndrome 4 (HPMRS4) | |
ELSAYED MOHAMED ALI, HAMOUD MOHAMED GALLAB |
XIA-GIBBS SYNDROME WITH PARTICULAR HAIR - A RARE CAUSE OF GLOBAL DEVELOPMENTAL DELAY | |
Diana Gabriela Barca, Cristina Minca, Mihaela Axente |
CHALLENGES IN CLINICAL INTERPRETATION OF NEW MUTATIONS IN RARE CONDITIONS | |
Diana Gabriela Barca, Sorina Mihaela Papuc, Carmen Burloiu, Aurora Arghir, Magdalena Budisteanu |
Molecular diagnosis and genetic counselling of X fragile Syndrome | |
Nouha Abdelmoula Bouayed, Sonda Kammoun, Fatma Abid, Balkiss Abdelmoula, Wafa Aloulou, Samir Aloulou |
Neurocritical care, Neurotrauma, Neuroprotection
Assessment of clinical follow-up and prognosis in acute neurological condition in pediatric patients managed in pediatric intensive care unit | |
Ece Naz Karakaya, Deniz Yüksel, Selman Kesici, Ayşe Aksoy, Ülkühan Öztoprak, Çigdem Genç Sel, Erhan Aksoy, Hülya Kayılıoğlu |
Early Post-Traumatic Seizures in PediatricTraumatic Brain Injury | |
Snehal Surana, Arpita Devbrata Adhikari, Vineet Kumar, Mona Gajre, Vidya M |
Native medicine use and lead poisoning in children | |
Renee Alce, Renee Alce, Padma Balaji, Ravikumar Krupanandan, Venkataraman Viswanathan, Bala Ramachandran |
Neuroradiology
Role of Fetal Neuroimaging in Congenital Cytomegalovirus Infection, with Postnatal Imaging Correlation. | |
Vinay Kandula, Rahul Nikam, Lauren Averill, Arabinda Choudhary |
Isolated mitochondrial complex IV (cytochrome c oxidase) deficiency mimicking ADEM | |
Amal Yousef Kentab, Mohammed Al-Nasser, Hamdy Hassan, Hisham El Khaldi |
Neuroimmunology
Autoantibodies normilize after a month in tonsilitis and persist in Sydenham's chorea | |
Hilla Ben-Pazi, Julie Stoner, Adi Aran, Kathy Alvarez, Madeleine W Cunningham |
Unsolved mystery:11-year-old patient with antibody negative immune-mediated necrotizing myopathy | |
Cemal Karakas, Jeetendra Sah, Yaacov Anziska, Yoshimi Hisamoto, Radha Giridharan, Joan Cracco, Alexandra Reznikov, Geetha Chari |
Paediatric Guillian-Barré Syndrome variants presenting with dysautonomia | |
Omar Abdel-mannan, Luigi D’Argenzio, Matthew Pitt, Felice D’Arco, Sanjay Bhate, Yael Hacohen, Marios Kaliakatsos |
Hemophagocytic Lymphohistiocytosis: A missed diagnosis in children with neurological manifestations | |
Marwa Saeed Abd Elmaksoud, Ahmed Adel Hassan Elbehairy, Asmaa Elsharkawy, Yasmine El Chazli |
Anti-MOG antibody related demyelinating diseases: Clinical-radiological spectrum and treatment experience | |
Hepsen Mine SERIN, Erdem Simsek, Seda Kanmaz, İpek Dokurel Cetin, Sanem Yılmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben |
Therapeutic plasma exchange in inflammatory demyelinating CNS syndromes in paediatric patients | |
Silvia Noemi Tenembaum, Andrea Savransky, Marina Huaman Rios, Silvana Liz Vergel, Mabel Castro Velasquez, Sara Perez Sierra, Gabriela Marcarian, Romina Alba, Ana Maria Pugliese |
Pediatric Acquired Demyelination Syndromes (ADS) profile in a Brazilian center | |
José Albino da Paz, Renata Paolilo, Samira Apostolos-Pereira, Dagoberto Callegaro, Ana Luiza Araújo, Douglas Sato, Carolina Medeiros Rimkus |
Clinical and Neuroradiological profile of Acute Disseminated Encephalomyelitis in 13 children at tertiary center in Saudi Arabia | |
Amal Yousef Kentab, Amal Y. Kentab, Mustafa AM. Salih, Hamdy H. Hassan, Mohammed Na N. Al-Nasser, Heba Y. El khashab |
Clinico-radiological correlation of Acquired Demyelination Syndromes(ADS) of central nervous system: A pediatric cohort | |
ANSHITA ARORA, SONAM KOTHARI, SHILPA KULKARNI, ANAITA HEGDE, KRISHANKUMAR SHAH |
Clinico-radiologic spectrum and outcome of pediatric demyelinating disorders – A retrospective study | |
Bidisha Banerjee, Muhammed Valikandy Hafis, Ullas V Acharya |
The Clinical Course of Children Younger than 7 Years of Age with Anti-N-methyl-D-aspartate Receptor Encephalitis | |
Hitha Vishwanath Amin, Sarah R Risen, Mered Parnes, Christian Michael Niedzwicki, Eyal Muscal |
Neurooncology
A randomized, double-blind, parallel group, placebo-controlled trial of metformin in tuberous sclerosis complex | |
Sam Amin, Andrew A Mallick, Hannah Edwards, Andrew Lux, Amjad Khan, Matthew Laugharne, Marcus Likeman, Finbar O'Callaghan |
Neuro-opthalmology
Congenital double elevator palsy with ptosis in a child | |
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Neurorehabilitation
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Stroke & Neurovascular Disorders
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Pediatric ischemic stroke associated to deficiency of adenosine deaminase 2 (DADA2). | |
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Intraarterial Embolectomy in Pediatric Arterial Ischemic Stroke | |
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Syndromic associations in a cohort of children with moyamoya phenomenon | |
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Prevalence of sleep-related breathing disorders in childhood stroke: A comparative study | |
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