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1994 5
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1998 7
1999 1
2000 3
2001 4
2002 4
2003 5
2004 1
2005 3
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2008 5
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159 results

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Quoted phrase not found in phrase index: "Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome"
Page 1
Epileptogenesis in tuberous sclerosis complex-related developmental and epileptic encephalopathy.
Aronica E, Specchio N, Luinenburg MJ, Curatolo P. Aronica E, et al. Brain. 2023 Jul 3;146(7):2694-2710. doi: 10.1093/brain/awad048. Brain. 2023. PMID: 36806388 Free PMC article. Review.
Pre-symptomatic administration of vigabatrin, a GABAergic drug, delays seizure onset and reduces the risk of a subsequent epileptic encephalopathy, such as infantile spasms syndrome or Lennox-Gastaut syndrome. ...Future trials are needed to optimize th …
Pre-symptomatic administration of vigabatrin, a GABAergic drug, delays seizure onset and reduces the risk of a subsequent epileptic e …
Update on Food protein-induced enterocolitis syndrome (FPIES).
Calvani M, Anania C, Bianchi A, D'Auria E, Cardinale F, Votto M, Martelli A, Tosca M, Chiappini E, Brambilla I, Miraglia Del Giudice M, Caffarelli C. Calvani M, et al. Acta Biomed. 2021 Nov 29;92(S7):e2021518. doi: 10.23750/abm.v92iS7.12394. Acta Biomed. 2021. PMID: 34842596 Free PMC article. Review.
Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE mediated food allergy (FA) characterized by delayed and severe gastrointestinal symptoms that typically occurs within the first year of life. ...Diagnosis of FPIES may be difficult, mainly due to the l …
Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE mediated food allergy (FA) characterized by delayed and sever …
SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.
Vlaskamp DRM, Shaw BJ, Burgess R, Mei D, Montomoli M, Xie H, Myers CT, Bennett MF, XiangWei W, Williams D, Maas SM, Brooks AS, Mancini GMS, van de Laar IMBH, van Hagen JM, Ware TL, Webster RI, Malone S, Berkovic SF, Kalnins RM, Sicca F, Korenke GC, van Ravenswaaij-Arts CMA, Hildebrand MS, Mefford HC, Jiang Y, Guerrini R, Scheffer IE. Vlaskamp DRM, et al. Neurology. 2019 Jan 8;92(2):e96-e107. doi: 10.1212/WNL.0000000000006729. Epub 2018 Dec 12. Neurology. 2019. PMID: 30541864 Free PMC article.
Of the 57 patients, 56 had epilepsy: generalized in 55, with focal seizures in 7 and infantile spasms in 1. Median seizure onset age was 2 years. A novel type of drop attack was identified comprising eyelid myoclonia evolving to a myoclonic-atonic (n = 5) or atonic (n = 8) …
Of the 57 patients, 56 had epilepsy: generalized in 55, with focal seizures in 7 and infantile spasms in 1. Median seizure onset age …
Diagnosis, Treatment and Prevention of Nutritional Anemia in Children: Recommendations of the Joint Committee of Pediatric Hematology-Oncology Chapter and Pediatric and Adolescent Nutrition Society of the Indian Academy of Pediatrics.
Chandra J, Dewan P, Kumar P, Mahajan A, Singh P, Dhingra B, Radhakrishnan N, Sharma R, Manglani M, Rawat AK, Gupta P, Gomber S, Bhat S, Gaikwad P, Elizabeth KE, Bansal D, Dubey AP, Shah N, Kini P, Trehan A, Datta K, Basavraja GV, Saxena V, Kumar RR. Chandra J, et al. Indian Pediatr. 2022 Oct 15;59(10):782-801. Indian Pediatr. 2022. PMID: 36263494 Free article.
Children with macrocytic anemia in whom a quick response to treatment is required, such as those with pancytopenia, severe anemia, developmental delay and infantile tremor syndrome, should be managed using parenteral vitamin B12. ...
Children with macrocytic anemia in whom a quick response to treatment is required, such as those with pancytopenia, severe anemia, developme …
Infantile spasms.
Zupanc ML. Zupanc ML. Expert Opin Pharmacother. 2003 Nov;4(11):2039-48. doi: 10.1517/14656566.4.11.2039. Expert Opin Pharmacother. 2003. PMID: 14596657 Review.
The majority of patients with infantile spasms have a poor prognosis with intractable epilepsy, severe developmental delays and/or significant cognitive impairments. Of all patients with infantile spasms, 70 - 90% have mental retardation. Furthermore, 20 - 50 …
The majority of patients with infantile spasms have a poor prognosis with intractable epilepsy, severe developmental delays an …
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension study.
Knupp KG, Scheffer IE, Ceulemans B, Sullivan J, Nickels KC, Lagae L, Guerrini R, Zuberi SM, Nabbout R, Riney K, Agarwal A, Lock M, Dai D, Farfel GM, Galer BS, Gammaitoni AR, Polega S, Davis R, Gil-Nagel A. Knupp KG, et al. Epilepsia. 2023 Jan;64(1):139-151. doi: 10.1111/epi.17431. Epub 2022 Nov 9. Epilepsia. 2023. PMID: 36196777 Free PMC article. Clinical Trial.
OBJECTIVE: This study was undertaken to evaluate the long-term safety and effectiveness of fenfluramine in patients with Lennox-Gastaut syndrome (LGS). METHODS: Eligible patients with LGS who completed a 14-week phase 3 randomized clinical trial enroll …
OBJECTIVE: This study was undertaken to evaluate the long-term safety and effectiveness of fenfluramine in patients with Lennox-Gastaut s
Biochemical mechanisms in pathogenesis of infantile epileptic spasm syndrome.
Riikonen R. Riikonen R. Seizure. 2023 Feb;105:1-9. doi: 10.1016/j.seizure.2023.01.004. Epub 2023 Jan 7. Seizure. 2023. PMID: 36634586 Free article. Review.
The molecular mechanisms leading to infantile epileptic spasm syndrome (IESS) remain obscure. The only common factor seems to be that the spasms are restricted to a limited period of infancy, during a certain maturational state. ...An altered maturational process ma …
The molecular mechanisms leading to infantile epileptic spasm syndrome (IESS) remain obscure. The only common factor seems to …
Infantile Spasms: Opportunities to Improve Care.
Messer R, Knupp KG. Messer R, et al. Semin Neurol. 2020 Apr;40(2):236-245. doi: 10.1055/s-0040-1705121. Epub 2020 Mar 6. Semin Neurol. 2020. PMID: 32143232 Review.
Infantile spasm (IS) is a distinct epilepsy syndrome characterized by epileptic spasms (the clinical seizure type) and hypsarrhythmia (the electrographic abnormality). ...Despite common misconceptions, even patients with identified etiologies or preexisting d
Infantile spasm (IS) is a distinct epilepsy syndrome characterized by epileptic spasms (the clinical seizure type) and
Vigabatrin for infantile spasms.
Pesaturo KA, Spooner LM, Belliveau P. Pesaturo KA, et al. Pharmacotherapy. 2011 Mar;31(3):298-311. doi: 10.1592/phco.31.3.298. Pharmacotherapy. 2011. PMID: 21361740 Review.
Infantile spasms describe a pediatric epilepsy syndrome characterized by frequent clusters of brief symmetric muscle contractions; the condition is often associated with developmental delay. When infantile spasms are accompanied by hypsarrhythmia on el
Infantile spasms describe a pediatric epilepsy syndrome characterized by frequent clusters of brief symmetric muscle contracti
Treatment of epileptic encephalopathies.
McTague A, Cross JH. McTague A, et al. CNS Drugs. 2013 Mar;27(3):175-84. doi: 10.1007/s40263-013-0041-6. CNS Drugs. 2013. PMID: 23397290 Review.
In this review, we discuss the ongoing debate regarding the significance of inter-ictal discharges and the impact of the seizures themselves on the cognitive delay or regression that is a common feature of these syndromes. The syndromes also differ in many wa …
In this review, we discuss the ongoing debate regarding the significance of inter-ictal discharges and the impact of the seizures themselves …
159 results