 Nervous System Malformations
"Nervous System Malformations" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis.
| Descriptor ID |
D009421
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| MeSH Number(s) |
C10.500 C16.131.666
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| Concept/Terms |
Nervous System Malformations- Nervous System Malformations
- Malformation, Nervous System
- Malformations, Nervous System
- Nervous System Malformation
- Abnormalities, Nervous System
- Abnormality, Nervous System
- Nervous System Abnormality
- Anomalies, Nervous System
- Anomaly, Nervous System
- Nervous System Anomaly
- Congenital Abnormalities, Nervous System
- Congenital Anomalies, Nervous System
- Nervous System Malformations, Congenital
- Malformations, Nervous System, Congenital
- Nervous System Abnormalities
- Nervous System Anomalies
- Nervous System Congenital Abnormalities
- Nervous System Congenital Malformations
- Abnormalities, Congenital, Nervous System
- Congenital Malformations, Nervous System
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Below are MeSH descriptors whose meaning is more general than "Nervous System Malformations".
Below are MeSH descriptors whose meaning is more specific than "Nervous System Malformations".
This graph shows the total number of publications written about "Nervous System Malformations" by people in this website by year, and whether "Nervous System Malformations" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 0 | 1 | | 2011 | 0 | 1 | 1 | | 2013 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nervous System Malformations" by people in Profiles.
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Hiatt SM, Trajkova S, Sebastiano MR, Partridge EC, Abidi FE, Anderson A, Ansar M, Antonarakis SE, Azadi A, Bachmann-Gagescu R, Bartuli A, Benech C, Berkowitz JL, Betti MJ, Brusco A, Cannon A, Caron G, Chen Y, Cochran ME, Coleman TF, Crenshaw MM, Cuisset L, Curry CJ, Darvish H, Demirdas S, Descartes M, Douglas J, Dyment DA, Elloumi HZ, Ermondi G, Faoucher M, Farrow EG, Felker SA, Fisher H, Hurst ACE, Joset P, Kelly MA, Kmoch S, Leadem BR, Lyons MJ, Macchiaiolo M, Magner M, Mandrile G, Mattioli F, McEown M, Meadows SK, Medne L, Meeks NJL, Montgomery S, Napier MP, Natowicz M, Newberry KM, Niceta M, Noskova L, Nowak CB, Noyes AG, Osmond M, Prijoles EJ, Pugh J, Pullano V, Qu?lin C, Rahimi-Aliabadi S, Rauch A, Redon S, Reymond A, Schwager CR, Sellars EA, Scheuerle AE, Shukarova-Angelovska E, Skraban C, Stolerman E, Sullivan BR, Tartaglia M, Thiffault I, Uguen K, Uma?a LA, van Bever Y, van der Crabben SN, van Slegtenhorst MA, Waisfisz Q, Washington C, Rodan LH, Myers RM, Cooper GM. Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype. Am J Hum Genet. 2023 02 02; 110(2):215-227.
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Meoded A, Kukreja M, Orman G, Boltshauser E, Huisman TAGM. Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome. Neuropediatrics. 2022 06; 53(3):195-199.
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Mao D, Reuter CM, Ruzhnikov MRZ, Beck AE, Farrow EG, Emrick LT, Rosenfeld JA, Mackenzie KM, Robak L, Wheeler MT, Burrage LC, Jain M, Liu P, Calame D, K?ry S, Sillesen M, Schmitz-Abe K, Tonduti D, Spaccini L, Iascone M, Genetti CA, Koenig MK, Graf M, Tran A, Alejandro M, Lee BH, Thiffault I, Agrawal PB, Bernstein JA, Bellen HJ, Chao HT. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. Am J Hum Genet. 2020 04 02; 106(4):570-583.
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Poretti A, Meoded A, Rossi A, Raybaud C, Huisman TA. Diffusion tensor imaging and fiber tractography in brain malformations. Pediatr Radiol. 2013 Jan; 43(1):28-54.
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Meoded A, Turan S, Harman C, Poretti A, Zinreich J, Huisman TA. Pre- and postnatal ultrasound and magnetic resonance imaging of intracranial extra-axial glioneuronal heterotopia. Fetal Diagn Ther. 2011; 30(4):314-6.
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Graf WD, Kayyali HR, Abdelmoity AT, Womelduff GL, Williams AR, Morriss MC. Incidental neuroimaging findings in nonacute headache. J Child Neurol. 2010 Oct; 25(10):1182-7.
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Magdaleno S, Keshvara L, Curran T. Rescue of ataxia and preplate splitting by ectopic expression of Reelin in reeler mice. Neuron. 2002 Feb 14; 33(4):573-86.
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