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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1945 1
1946 1
1947 1
1948 1
1950 1
1951 3
1952 1
1954 1
1955 4
1956 3
1957 3
1958 6
1959 4
1960 1
1961 4
1962 10
1963 24
1964 10
1965 14
1966 26
1967 22
1968 24
1969 23
1970 26
1971 40
1972 27
1973 19
1974 38
1975 122
1976 131
1977 133
1978 131
1979 161
1980 181
1981 161
1982 224
1983 221
1984 240
1985 238
1986 237
1987 245
1988 228
1989 313
1990 356
1991 335
1992 347
1993 437
1994 486
1995 453
1996 449
1997 532
1998 585
1999 644
2000 654
2001 744
2002 762
2003 828
2004 996
2005 1134
2006 1313
2007 1593
2008 1721
2009 1791
2010 1971
2011 2181
2012 2526
2013 2800
2014 2798
2015 2861
2016 3071
2017 3216
2018 3310
2019 3533
2020 3599
2021 3800
2022 3475
2023 3029
2024 1102

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52,810 results

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Quoted phrase not found in phrase index: "Neurodevelopmental disorder with or without seizures and gait abnormalities"
Page 1
Neurodevelopmental disorders.
Thapar A, Cooper M, Rutter M. Thapar A, et al. Lancet Psychiatry. 2017 Apr;4(4):339-346. doi: 10.1016/S2215-0366(16)30376-5. Epub 2016 Dec 13. Lancet Psychiatry. 2017. PMID: 27979720 Review.
Neurodevelopmental disorders such as attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder, although most commonly considered in childhood, can be lifelong conditions. ...Overall, we argue strongly for a flexible approach in clin …
Neurodevelopmental disorders such as attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder …
Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders.
Turner TN, Wilfert AB, Bakken TE, Bernier RA, Pepper MR, Zhang Z, Torene RI, Retterer K, Eichler EE. Turner TN, et al. Am J Hum Genet. 2019 Dec 5;105(6):1274-1285. doi: 10.1016/j.ajhg.2019.11.003. Epub 2019 Nov 27. Am J Hum Genet. 2019. PMID: 31785789 Free PMC article.
While genes with an excess of de novo mutations (DNMs) have been identified in children with neurodevelopmental disorders (NDDs), few studies focus on DNM patterns where the sex of affected children is examined separately. ...A replication cohort of 18,778 sequenced …
While genes with an excess of de novo mutations (DNMs) have been identified in children with neurodevelopmental disorders (NDD …
Neurodevelopmental disorders-the history and future of a diagnostic concept.
Morris-Rosendahl DJ, Crocq MA. Morris-Rosendahl DJ, et al. Dialogues Clin Neurosci. 2020 Mar;22(1):65-72. doi: 10.31887/DCNS.2020.22.1/macrocq. Dialogues Clin Neurosci. 2020. PMID: 32699506 Free PMC article. Review.
This article describes the history of the diagnostic class of neurodevelopmental disorders (NDDs) up to DSM-5. We further analyze how the development of genetics will transform the classification and diagnosis of NDDs. ...Genetic research supports the hypothesis tha …
This article describes the history of the diagnostic class of neurodevelopmental disorders (NDDs) up to DSM-5. We further anal …
Prenatal stress: Effects on fetal and child brain development.
Lautarescu A, Craig MC, Glover V. Lautarescu A, et al. Int Rev Neurobiol. 2020;150:17-40. doi: 10.1016/bs.irn.2019.11.002. Epub 2019 Dec 14. Int Rev Neurobiol. 2020. PMID: 32204831 Review.
These include depression, anxiety, Attention Deficit Hyperactivity Disorder (ADHD), and/or conduct disorders. There is an increased risk for other outcomes also, including preterm delivery and reduced telomere length, possibly indicative of an accelerated life histo …
These include depression, anxiety, Attention Deficit Hyperactivity Disorder (ADHD), and/or conduct disorders. There is an incr …
The Cerebellum and Neurodevelopmental Disorders.
Stoodley CJ. Stoodley CJ. Cerebellum. 2016 Feb;15(1):34-37. doi: 10.1007/s12311-015-0715-3. Cerebellum. 2016. PMID: 26298473 Free PMC article. Review.
Cerebellar dysfunction is evident in several developmental disorders, including autism, attention deficit-hyperactivity disorder (ADHD), and developmental dyslexia, and damage to the cerebellum early in development can have long-term effects on movement, cognition, …
Cerebellar dysfunction is evident in several developmental disorders, including autism, attention deficit-hyperactivity disorder …
Diagnosis and Treatment of Cyclothymia: The "Primacy" of Temperament.
Perugi G, Hantouche E, Vannucchi G. Perugi G, et al. Curr Neuropharmacol. 2017 Apr;15(3):372-379. doi: 10.2174/1570159X14666160616120157. Curr Neuropharmacol. 2017. PMID: 28503108 Free PMC article. Review.
METHOD: In the present article, we critically reviewed the literature on the diagnosis and treatment of cyclothymia, focusing on the temperamental and neurodevelopmental perspectives. RESULTS: Current epidemiological and clinical research showed the high prevalence and the …
METHOD: In the present article, we critically reviewed the literature on the diagnosis and treatment of cyclothymia, focusing on the tempera …
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.
Langhammer F, Maroofian R, Badar R, Gregor A, Rochman M, Ratliff JB, Koopmans M, Herget T, Hempel M, Kortüm F, Heron D, Mignot C, Keren B, Brooks S, Botti C, Ben-Zeev B, Argilli E, Sherr EH, Gowda VK, Srinivasan VM, Bakhtiari S, Kruer MC, Salih MA, Kuechler A, Muller EA, Blocker K, Kuismin O, Park KL, Kochhar A, Brown K, Ramanathan S, Clark RD, Elgizouli M, Melikishvili G, Tabatadze N, Stark Z, Mirzaa GM, Ong J, Grasshoff U, Bevot A, von Wintzingerode L, Jamra RA, Hennig Y, Goldenberg P, Al Alam C, Charif M, Boulouiz R, Bellaoui M, Amrani R, Al Mutairi F, Tamim AM, Abdulwahab F, Alkuraya FS, Khouj EM, Alvi JR, Sultan T, Hashemi N, Karimiani EG, Ashrafzadeh F, Imannezhad S, Efthymiou S, Houlden H, Sticht H, Zweier C. Langhammer F, et al. Genet Med. 2023 Aug;25(8):100885. doi: 10.1016/j.gim.2023.100885. Epub 2023 May 8. Genet Med. 2023. PMID: 37165955
PURPOSE: Missense variants clustering in the BTB domain region of RHOBTB2 cause a developmental and epileptic encephalopathy with early-onset seizures and severe intellectual disability. METHODS: By international collaboration, we assembled individuals with pathogenic RHOB …
PURPOSE: Missense variants clustering in the BTB domain region of RHOBTB2 cause a developmental and epileptic encephalopathy with early-onse …
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD.
Pavinato L, Delle Vedove A, Carli D, Ferrero M, Carestiato S, Howe JL, Agolini E, Coviello DA, van de Laar I, Au PYB, Di Gregorio E, Fabbiani A, Croci S, Mencarelli MA, Bruno LP, Renieri A, Veltra D, Sofocleous C, Faivre L, Mazel B, Safraou H, Denommé-Pichon AS, van Slegtenhorst MA, Giesbertz N, van Jaarsveld RH, Childers A, Rogers RC, Novelli A, De Rubeis S, Buxbaum JD, Scherer SW, Ferrero GB, Wirth B, Brusco A. Pavinato L, et al. Brain. 2023 Feb 13;146(2):534-548. doi: 10.1093/brain/awac278. Brain. 2023. PMID: 35979925 Free PMC article.
We identified 12 cases with loss-of-function CAPRIN1 variants, and a neurodevelopmental phenotype characterized by language impairment/speech delay (100%), intellectual disability (83%), attention deficit hyperactivity disorder (82%) and autism spectrum disorder …
We identified 12 cases with loss-of-function CAPRIN1 variants, and a neurodevelopmental phenotype characterized by language impairmen …
Association between plasma proteome and childhood neurodevelopmental disorders: A two-sample Mendelian randomization analysis.
Yang J, He X, Qian L, Zhao B, Fan Y, Gao F, Yan B, Zhu F, Ma X. Yang J, et al. EBioMedicine. 2022 Apr;78:103948. doi: 10.1016/j.ebiom.2022.103948. Epub 2022 Mar 17. EBioMedicine. 2022. PMID: 35306338 Free PMC article.
BACKGROUND: Childhood neurodevelopmental disorders, including autism spectrum disorder (ASD), attention-deficit hyperactivity disorder (ADHD), and Tourette syndrome (TS), comprise a major cause of health-related disabilities in children. ...The causal …
BACKGROUND: Childhood neurodevelopmental disorders, including autism spectrum disorder (ASD), attention-deficit hyperac …
DLG4-related synaptopathy: a new rare brain disorder.
Rodríguez-Palmero A, Boerrigter MM, Gómez-Andrés D, Aldinger KA, Marcos-Alcalde Í, Popp B, Everman DB, Lovgren AK, Arpin S, Bahrambeigi V, Beunders G, Bisgaard AM, Bjerregaard VA, Bruel AL, Challman TD, Cogné B, Coubes C, de Man SA, Denommé-Pichon AS, Dye TJ, Elmslie F, Feuk L, García-Miñaúr S, Gertler T, Giorgio E, Gruchy N, Haack TB, Haldeman-Englert CR, Haukanes BI, Hoyer J, Hurst ACE, Isidor B, Soller MJ, Kushary S, Kvarnung M, Landau YE, Leppig KA, Lindstrand A, Kleinendorst L, MacKenzie A, Mandrile G, Mendelsohn BA, Moghadasi S, Morton JE, Moutton S, Müller AJ, O'Leary M, Pacio-Míguez M, Palomares-Bralo M, Parikh S, Pfundt R, Pode-Shakked B, Rauch A, Repnikova E, Revah-Politi A, Ross MJ, Ruivenkamp CAL, Sarrazin E, Savatt JM, Schlüter A, Schönewolf-Greulich B, Shad Z, Shaw-Smith C, Shieh JT, Shohat M, Spranger S, Thiese H, Mau-Them FT, van Bon B, van de Burgt I, van de Laar IMBH, van Drie E, van Haelst MM, van Ravenswaaij-Arts CM, Verdura E, Vitobello A, Waldmüller S, Whiting S, Zweier C, Prada CE, de Vries BBA, Dobyns WB, Reiter SF, Gómez-Puertas P, Pujol A, Tümer Z. Rodríguez-Palmero A, et al. Genet Med. 2021 May;23(5):888-899. doi: 10.1038/s41436-020-01075-9. Epub 2021 Feb 17. Genet Med. 2021. PMID: 33597769 Free article.
RESULTS: The clinical picture was predominated by early onset global developmental delay, intellectual disability, autism spectrum disorder, and attention deficit-hyperactivity disorder, all of which point to a brain disorder. ...CONCLUSION: The present study …
RESULTS: The clinical picture was predominated by early onset global developmental delay, intellectual disability, autism spectrum disord …
52,810 results
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