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    August 2021
  1. MADAAN P, Kaur A, Saini L, Paria P, et al
    PPP2R5D-Related Neurodevelopmental Disorder or Developmental and Epileptic Encephalopathy?: A Novel Phenotypic Description and Review of Published Cases.
    Neuropediatrics. 2021 Aug 26. doi: 10.1055/s-0041-1733984.
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    July 2021
  2. STERN T, Kornreich L, Goldberg H
    Yield of Brain Magnetic Resonance Imaging in Epilepsy Diagnosis from 1998 to 2020: A Large Retrospective Cohort Study.
    Neuropediatrics. 2021 Jul 29. doi: 10.1055/s-0041-1732325.
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  3. VON STULPNAGEL C, Kutschker S, Sperl W, Berweck S, et al
    Childhood Stroke: Long-Term Outcomes and Health-Related Quality of Life with a Special Focus on the Development of Epilepsy.
    Neuropediatrics. 2021 Jul 12. doi: 10.1055/s-0041-1731805.
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    June 2021
  4. SAVAGE MC, Kielian A, Elitt C, Peters JM, et al
    Startle Epilepsy Triggered By Maternal Cough.
    Neuropediatrics. 2021 Jun 30. doi: 10.1055/s-0041-1731008.
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    April 2021
  5. SIDDIQUI A, McGregor AL, Wheless JW, Klimo P, et al
    Utility of Epilepsy Surgery in Survivors of Childhood Cancer.
    Neuropediatrics. 2021 Apr 14. doi: 10.1055/s-0041-1728653.
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    Epilepsy in Neuropediatrics.
    Neuropediatrics. 2021;52:71-72.
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    February 2021
  7. MASTRANGELO M, Commone C, Greco C, Leuzzi V, et al
    TSC1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Child with a Mild Phenotype of Tuberous Sclerosis.
    Neuropediatrics. 2021 Feb 12. doi: 10.1055/s-0041-1722881.
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  8. HOFMEISTER B, von Stulpnagel C, Betzler C, Mari F, et al
    Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects.
    Neuropediatrics. 2021 Feb 12. doi: 10.1055/s-0041-1722878.
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    January 2021
  9. BOSSI G, Bruno R, Novati S, Maserati R, et al
    Cerebral Toxocariasis as a Cause of Epilepsy: A Pediatric Case.
    Neuropediatrics. 2021 Jan 20. doi: 10.1055/s-0040-1721701.
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  10. KO PY, Glass IA, Crandall S, Weiss A, et al
    Two Missense CACNA1A Variants in a Single Family with Variable Neurobehavioral, Cerebellar, Epileptic, and Oculomotor Features.
    Neuropediatrics. 2021 Jan 14. doi: 10.1055/s-0040-1721686.
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    December 2020
    Pediatric Epilepsy Surgery: Preoperative Assessment and Surgical Treatment.
    Neuropediatrics. 2020 Dec 22. doi: 10.1055/s-0040-1721829.
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    November 2020
  12. BABA S, Okanishi T, Ohsugi K, Suzumura R, et al
    Possible Role of High-Dose Barbiturates and Early Administration of Parenteral Ketogenic Diet for Reducing Development of Chronic Epilepsy in Febrile Infection-Related Epilepsy Syndrome: A Case Report.
    Neuropediatrics. 2020 Nov 23. doi: 10.1055/s-0040-1716903.
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    October 2020
  13. VETRI L, Cali F, Vinci M, Amato C, et al
    Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy".
    Neuropediatrics. 2020 Oct 27. doi: 10.1055/s-0040-1716904.
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  14. WILLIMSKY EK, Munzig A, Mayer K, Biskup S, et al
    Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.
    Neuropediatrics. 2020 Oct 21. doi: 10.1055/s-0040-1712488.
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    August 2020
  15. CLOPPENBORG T, Albers K, Kalbhenn T, Woermann FG, et al
    Hyperkinetic Seizures with Ictal Fear as Localizing Ictal Signs in MRI-Negative Medial Frontal Lobe Epilepsy.
    Neuropediatrics. 2020 Aug 25. doi: 10.1055/s-0040-1715630.
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    May 2020
  16. RADEMACHER A, Schwarz N, Seiffert S, Pendziwiat M, et al
    Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy.
    Neuropediatrics. 2020 May 11. doi: 10.1055/s-0040-1710524.
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    April 2020
  17. HANCI F, Turay S, Balci P, Kabakus N, et al
    Reflex Epilepsy with Hot Water: Clinical and EEG Findings, Treatment, and Prognosis in Childhood.
    Neuropediatrics. 2020 Apr 15. doi: 10.1055/s-0040-1709455.
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    Changing Landscape of Dravet Syndrome Management: An Overview.
    Neuropediatrics. 2020;51:135-145.
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  19. VAN BEUSICHEM AE, Nicolai J, Verhoeven J, Speth L, et al
    Mobility Characteristics of Children with Spastic Paraplegia Due to a Mutation in the KIF1A Gene.
    Neuropediatrics. 2020;51:146-153.
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  20. PFEIFFER B, Sen K, Kaur S, Pappas K, et al
    Expanding Phenotypic Spectrum of Cerebral Aspartate-Glutamate Carrier Isoform 1 (AGC1) Deficiency.
    Neuropediatrics. 2020;51:160-163.
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    March 2020
  21. KHARYTONOV V, Dulac O
    Are Epileptic Spasms a Seizure Type for the Insular Region?
    Neuropediatrics. 2020 Mar 28. doi: 10.1055/s-0040-1702226.
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    February 2020
    Ketamine Infusion for Super Refractory Status Epilepticus in Alternating Hemiplegia of Childhood.
    Neuropediatrics. 2020 Feb 3. doi: 10.1055/s-0039-3402005.
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  23. NAGY E, Farkas N, Hollody K
    Does Co-occurred Cerebral Palsy Change the Prognosis of West Syndrome?
    Neuropediatrics. 2020;51:30-36.
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  24. KORTAS A, Schiller K, Unterholzner G, Rauchenzauner M, et al
    Accuracy of Flash Glucose Monitoring in a Patient with Dravet Syndrome on a Ketogenic Diet.
    Neuropediatrics. 2020;51:45-48.
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  25. HORNEMANN F, Le Duc D, Roth C, Pfaffle R, et al
    Childhood Dystonia-Parkinsonism Following Infantile Spasms-Clinical Clue to Diagnosis in Early Beta-Propeller Protein-Associated Neurodegeneration.
    Neuropediatrics. 2020;51:22-29.
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    November 2019
  26. VALOVA V, Kochan A, Werry B, John R, et al
    Early Onset, Long Illness Duration, Epilepsy Type, and Polypharmacy Have an Adverse Effect on Psychosocial Outcome in Children with Epilepsy.
    Neuropediatrics. 2019 Nov 21. doi: 10.1055/s-0039-3399529.
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    September 2019
  27. ZHANG Y, Zhang L, Zhou S
    Developmental Regression and Epilepsy of Infancy with Migrating Focal Seizures Caused by TBCD Mutation: A Case Report and Review of the Literature.
    Neuropediatrics. 2019 Sep 30. doi: 10.1055/s-0039-1698423.
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  28. HOPMANS EM, van der Heide A, Chung PK, Brinkman D, et al
    Rotavirus-Induced Neonatal Epileptic Encephalopathy-A Disease Spectrum Illustrated by Monochorionic Twins.
    Neuropediatrics. 2019 Sep 21. doi: 10.1055/s-0039-1695712.
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    July 2019
  29. GIACOMINI T, Vari MS, Janis S, Prato G, et al
    Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene.
    Neuropediatrics. 2019 Jul 18. doi: 10.1055/s-0039-1692141.
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  30. BAMBORSCHKE D, Pergande M, Daimaguler HS, Mangold E, et al
    Cleft Palate as Distinguishing Feature in a Patient with GABRB3 Epileptic Encephalopathy.
    Neuropediatrics. 2019 Jul 18. doi: 10.1055/s-0039-1693143.
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    April 2019
  31. SCHMID SJ, Wagner M, Goetz C, Makowski C, et al
    A De Novo Dominant Negative Mutation in DNM1L Causes Sudden Onset Status Epilepticus with Subsequent Epileptic Encephalopathy.
    Neuropediatrics. 2019 Apr 2. doi: 10.1055/s-0039-1685217.
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  32. ISHIKAWA N, Tani H, Kobayashi Y, Kato A, et al
    High Incidence of Renal Stones in Severely Disabled Children with Epilepsy Treated with Topiramate.
    Neuropediatrics. 2019 Apr 2. doi: 10.1055/s-0038-1676287.
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    March 2019
  33. KLUGER G, von Stulpnagel-Steinbeis C, Arnold S, Eschermann K, et al
    Positive Short-Term Effect of Low-Dose Rosuvastatin in a Patient with SYNGAP1-Associated Epilepsy.
    Neuropediatrics. 2019 Mar 15. doi: 10.1055/s-0039-1681066.
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    December 2018
  34. SEDLACKOVA L, Lassuthova P, Sterbova K, Haberlova J, et al
    UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood.
    Neuropediatrics. 2018 Dec 5. doi: 10.1055/s-0038-1676288.
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    August 2018
  35. KOVACS-NAGY R, Morin G, Nouri MA, Brandau O, et al
    HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 Patients.
    Neuropediatrics. 2018 Aug 16. doi: 10.1055/s-0038-1667345.
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    July 2018
  36. YOUNES TB, Benrhouma H, Klaa H, Rouissi A, et al
    Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review.
    Neuropediatrics. 2018 Jul 16. doi: 10.1055/s-0038-1667024.
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  37. GULIYEVA U, Okur I, Dulac O, Khalilov O, et al
    Epilepsy in Biotinidase Deficiency Is Distinct from Early Myoclonic Encephalopathy.
    Neuropediatrics. 2018 Jul 12. doi: 10.1055/s-0038-1666845.
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  38. TAN AP
    Febrile Infection-Related Epilepsy Syndrome (FIRES) with Multifocal Subcortical Infarcts, A New Imaging Phenotype.
    Neuropediatrics. 2018 Jul 6. doi: 10.1055/s-0038-1661418.
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    May 2018
  39. HOLZE N, Baalen AV, Stephani U, Helbig I, et al
    Variants in the ATP1A3 Gene Mutations within Severe Apnea Starting in Early Infancy: An Observational Study of Two Cases with a Possible Relation to Epileptic Activity.
    Neuropediatrics. 2018 May 25. doi: 10.1055/s-0038-1653978.
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  40. AL DHAIBANI MA, El-Hattab AW, Ismayl O, Suleiman J, et al
    B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss.
    Neuropediatrics. 2018 May 23. doi: 10.1055/s-0038-1651519.
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    April 2018
  41. LIN Q, Yang PF, Jia YZ, Pei JS, et al
    Surgical Treatment and Long-Term Outcome of Cerebral Cavernous Malformations-Related Epilepsy in Pediatric Patients.
    Neuropediatrics. 2018 Apr 20. doi: 10.1055/s-0038-1645871.
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    Microsurgery in Cavernoma-Related Epilepsy in Children: Do Results in Children Differ from Adults?
    Neuropediatrics. 2018 Apr 20. doi: 10.1055/s-0038-1645873.
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  43. PISCIOTTA L, Capra V, Accogli A, Giacomini T, et al
    Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral Phenotype.
    Neuropediatrics. 2018 Apr 9. doi: 10.1055/s-0038-1639372.
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    February 2018
  44. STERBOVA K, Vlckova M, Klement P, Neupauerova J, et al
    Neonatal Onset of Epilepsy of Infancy with Migrating Focal Seizures Associated with a Novel GABRB3 Variant in Monozygotic Twins.
    Neuropediatrics. 2018 Feb 14. doi: 10.1055/s-0038-1626708.
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  45. SRINIVASARAGHAVAN R, Parameswaran N, Mathis D, Burer C, et al
    Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings.
    Neuropediatrics. 2018 Feb 5. doi: 10.1055/s-0037-1621721.
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    January 2018
    Erratum: Cognition and Behavior in Childhood Epilepsy.
    Neuropediatrics. 2018 Jan 4. doi: 10.1055/s-0037-1621744.
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    December 2017
  47. KANEMURA H, Sano F, Ohyama T, Sugita K, et al
    Effect of Levetiracetam Monotherapy in Nonlesional Focal Childhood Epilepsy.
    Neuropediatrics. 2017 Dec 18. doi: 10.1055/s-0037-1613680.
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  48. RAMANTANI G, Reuner G
    Cognitive Development in Pediatric Epilepsy Surgery.
    Neuropediatrics. 2017 Dec 5. doi: 10.1055/s-0037-1609034.
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    September 2017
  49. ERKENT I, Gocmen R, Tezer FI, Oguz KK, et al
    Postherpetic Anti-N-methyl-D-aspartate Receptor Encephalitis after Hemispherotomy in a Patient with Intractable Startle Epilepsy.
    Neuropediatrics. 2017 Sep 22. doi: 10.1055/s-0037-1606640.
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  50. WAGNER M, Gusic M, Gunthner R, Alhaddad B, et al
    Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related Epilepsy.
    Neuropediatrics. 2017 Sep 15. doi: 10.1055/s-0037-1606370.
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    August 2017
  51. BOLSTERLI HEINZLE BK, Bast T, Critelli H, Huber R, et al
    Erratum: Age-Dependency of Location of Epileptic Foci in "Continuous Spike-and-Waves during Sleep": A Parallel to the Posterior-Anterior Trajectory of Slow Wave Activity.
    Neuropediatrics. 2017 Aug 4. doi: 10.1055/s-0037-1602427.
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    June 2017
  52. KOMULAINEN-EBRAHIM J, Saastamoinen E, Rahikkala E, Helander H, et al
    Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis.
    Neuropediatrics. 2017 Jun 30. doi: 10.1055/s-0037-1603976.
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    The Epilepsy-Aphasia Spectrum: From Landau-Kleffner Syndrome to Rolandic Epilepsy.
    Neuropediatrics. 2017 Jun 19. doi: 10.1055/s-0037-1603962.
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  54. DARWISH AH, Alshahawy AK, El-Shehaby WA
    Epileptiform Activity in Electroencephalogram of Normal Children.
    Neuropediatrics. 2017 Jun 5. doi: 10.1055/s-0037-1603514.
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    Lennox-Gastaut Syndrome: A State of the Art Review.
    Neuropediatrics. 2017;48:143-151.
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  56. TOUNTOPOULOU M, Weschke B, Kaindl AM
    Lacosamide Lowers Valproate and Levetiracetam Levels.
    Neuropediatrics. 2017;48:188-189.
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    April 2017
  57. KLOTZ KA, Lemke JR, Korinthenberg R, Jacobs J, et al
    Vitamin B6-Responsive Epilepsy due to a Novel KCNQ2 Mutation.
    Neuropediatrics. 2017 Apr 18. doi: 10.1055/s-0037-1601857.
    >> Share

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