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

Year Number of Results
1973 1
1974 1
1975 1
1976 2
1977 1
1978 1
1979 1
1980 1
1981 3
1982 2
1983 6
1984 1
1985 5
1986 4
1987 7
1988 6
1989 3
1990 6
1991 3
1992 9
1993 14
1994 10
1995 10
1996 9
1997 11
1998 13
1999 16
2000 11
2001 20
2002 11
2003 9
2004 9
2005 18
2006 15
2007 18
2008 14
2009 21
2010 18
2011 21
2012 21
2013 30
2014 18
2015 20
2016 20
2017 17
2018 10
2019 23
2020 23
2021 16
2022 16
2023 23
2024 6

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513 results

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Quoted phrase not found in phrase index: "Hypoplasia of the pons"
Page 1
Tubulin mutations in human neurodevelopmental disorders.
Maillard C, Roux CJ, Charbit-Henrion F, Steffann J, Laquerriere A, Quazza F, Buisson NB. Maillard C, et al. Semin Cell Dev Biol. 2023 Mar 15;137:87-95. doi: 10.1016/j.semcdb.2022.07.009. Epub 2022 Jul 30. Semin Cell Dev Biol. 2023. PMID: 35915025 Review.
Additional distinctive MRI features include dysmorphism of the basal ganglia, midline commissural structure hypoplasia or agenesis, and cerebellar and brainstem hypoplasia. Tubulinopathies can be diagnosed as early as 21-24 gestational weeks using imaging and neurop …
Additional distinctive MRI features include dysmorphism of the basal ganglia, midline commissural structure hypoplasia or agenesis, a …
Tension-type headache.
Mathew NT. Mathew NT. Curr Neurol Neurosci Rep. 2006 Mar;6(2):100-5. doi: 10.1007/s11910-996-0031-x. Curr Neurol Neurosci Rep. 2006. PMID: 16522262 Review.
Future treatment modalities are likely to be based on such mechanisms. Using MRI and voxel-based morphometry, structural abnormalities have been found in patients with CTTH for the first time. Pain processing areas such as dorsal rostral and ventral pons, anterior c …
Future treatment modalities are likely to be based on such mechanisms. Using MRI and voxel-based morphometry, structural abnormalities …
See-saw nystagmus.
Williams IM, Dickinson P, Ramsay RJ, Thomas L. Williams IM, et al. Aust J Ophthalmol. 1982 Feb;10(1):19-25. Aust J Ophthalmol. 1982. PMID: 7103859
We suggest a lesion impairing the function of that circuitry of cells thought to include the nucleus centromedianus of the thalamus, the zona incerta, the interstitial nucleus of Cajal and eye movement related cells in the mid brain and pons, causes the disconjugate eye mo …
We suggest a lesion impairing the function of that circuitry of cells thought to include the nucleus centromedianus of the thalamus, the zon …
Locked-in syndrome.
Cardwell MS. Cardwell MS. Tex Med. 2013 Feb 1;109(2):e1. Tex Med. 2013. PMID: 23378122
Etiologies of locked-in syndrome include hemorrhagic and thrombotic events, tumors affecting the ventral pons, infectious agents, iatrogenic causes, trauma, metabolic abnormalities, and other miscellaneous causes. ...
Etiologies of locked-in syndrome include hemorrhagic and thrombotic events, tumors affecting the ventral pons, infectious agents, iat …
Radiosurgery for brainstem arteriovenous malformation.
Maruyama K, Koga T, Niranjan A, Kondziolka D, Flickinger JC, Lunsford LD. Maruyama K, et al. Prog Neurol Surg. 2013;27:67-72. doi: 10.1159/000341639. Epub 2012 Dec 11. Prog Neurol Surg. 2013. PMID: 23258510 Review.
The majority of patients with brainstem AVMs had a history of hemorrhage, leading to neurological deficits at the time of treatment in 72-73% of patients. The most frequent location was the midbrain or the pons depending on studies, while the medulla oblongata was the leas …
The majority of patients with brainstem AVMs had a history of hemorrhage, leading to neurological deficits at the time of treatment in 72-73 …
Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly.
Krajden Haratz K, Oliveira Szejnfeld P, Govindaswamy M, Leibovitz Z, Gindes L, Severino M, Rossi A, Paladini D, Garcia Rodriguez R, Ben-Sira L, Borkowski Tillman T, Gupta R, Lotem G, Raz N, Hamamoto TENK, Kidron D, Arad A, Birnbaum R, Brussilov M, Pomar L, Vial Y, Leventer RJ, McGillivray G, Fink M, Krzeszowski W, Fernandes Moron A, Lev D, Tamarkin M, Shalev J, Har Toov J, Lerman-Sagie T, Malinger G. Krajden Haratz K, et al. Ultrasound Obstet Gynecol. 2021 Dec;58(6):864-874. doi: 10.1002/uog.23660. Ultrasound Obstet Gynecol. 2021. PMID: 33942916 Free article.
Infratentorially, the fourth ventricle was abnormal in 88.7% of cases overall, and anomalies of the midbrain and pons were frequent (93.5% and 77.4%, respectively). Ventriculomegaly was observed in 80.6% of all cases, being more severe in cases with complete RES than in th …
Infratentorially, the fourth ventricle was abnormal in 88.7% of cases overall, and anomalies of the midbrain and pons were frequent ( …
Brainstem disconnection.
Duffield C, Jocson J, Wootton-Gorges SL. Duffield C, et al. Pediatr Radiol. 2009 Dec;39(12):1357-60. doi: 10.1007/s00247-009-1378-3. Epub 2009 Aug 11. Pediatr Radiol. 2009. PMID: 19669743 Free PMC article.
We report a unique case of a neonate who presented at delivery with hypertonia, dysmorphic facial features, and respiratory distress, as well as numerous musculoskeletal and genitourinary abnormalities. MRI of the brain showed disconnection between the pons and medu …
We report a unique case of a neonate who presented at delivery with hypertonia, dysmorphic facial features, and respiratory distress, as wel …
Brain Magnetic Resonance Imaging Abnormalities in Acute Flaccid Myelitis.
Caceres JA, Saucier L, Murphy OC, Gordon-Lipkin EM, Santoro JD, Van Haren K, Pardo CA, Hopkins S. Caceres JA, et al. Pediatr Neurol. 2023 Dec;149:56-62. doi: 10.1016/j.pediatrneurol.2023.08.021. Epub 2023 Aug 19. Pediatr Neurol. 2023. PMID: 37797356 Review.
RESULTS: A total of 66 patients were included. Brain MRI abnormalities were present in 34 (52%). Infratentorial abnormalities were more common, occurring in 33 (97%) cases with the dorsal pons being the most frequently affected area (88%). Abnormalities …
RESULTS: A total of 66 patients were included. Brain MRI abnormalities were present in 34 (52%). Infratentorial abnormalities …
Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasia.
Namavar Y, Barth PG, Poll-The BT, Baas F. Namavar Y, et al. Orphanet J Rare Dis. 2011 Jul 12;6:50. doi: 10.1186/1750-1172-6-50. Orphanet J Rare Dis. 2011. PMID: 21749694 Free PMC article. Review.
Pontocerebellar Hypoplasia (PCH) is group of very rare, inherited progressive neurodegenerative disorders with prenatal onset. ...The incidence of each subtype is unknown. All subtypes share common characteristics, including hypoplasia/atrophy of cerebellum and p …
Pontocerebellar Hypoplasia (PCH) is group of very rare, inherited progressive neurodegenerative disorders with prenatal onset. ...The …
Human malformations of the midbrain and hindbrain: review and proposed classification scheme.
Parisi MA, Dobyns WB. Parisi MA, et al. Mol Genet Metab. 2003 Sep-Oct;80(1-2):36-53. doi: 10.1016/j.ymgme.2003.08.010. Mol Genet Metab. 2003. PMID: 14567956 Review.
We consider the heterogeneous entity of cerebellar vermis hypoplasia and describe the recently identified gene associated with an X-linked form of this condition. Finally, the pontocerebellar hypoplasias are discussed in the context of their generally progressive de …
We consider the heterogeneous entity of cerebellar vermis hypoplasia and describe the recently identified gene associated with an X-l …
513 results