Matthew T Whitehead
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Explore the profile of Matthew T Whitehead including associated specialties, affiliations and a list of published articles.
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110
Citations
644
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Recent Articles
1.
Russ J, Agarwal S, Venkatesan C, Scelsa B, Vollmer B, Tarui T, et al.
Brain
. 2025 Mar;
PMID: 40048696
Malformations of cortical development (MCDs) are a heterogeneous family of congenital brain malformations that originate from disturbed development of the cerebral cortex. MCDs can arise from primary genetic disorders that...
2.
Martinez-Correa S, Rafful P, Ramirez-Suarez K, Viaene A, Beslow L, Agarwal S, et al.
AJNR Am J Neuroradiol
. 2025 Feb;
PMID: 39952664
Background And Purpose: Subpial hemorrhage is an underrecognized type of hemorrhagic stroke primarily affecting neonates. Blood accumulation in the impermeable pia mater compresses the adjacent cortex, leading to injury. The...
3.
Whitehead M, Manteghinejad A, Alves C, Simsek O, Khalek N, Schwartz E
AJNR Am J Neuroradiol
. 2025 Jan;
PMID: 39794134
Background And Purpose: Frontal paraventricular cystic changes have a varied etiology that includes connatal cysts, subependymal pseudocysts, necrosis, and enlarged perivascular spaces. These may be difficult to distinguish by neuroimaging...
4.
Ouyang M, Whitehead M, Mohapatra S, Zhu T, Huang H
Semin Fetal Neonatal Med
. 2024 Nov;
29(2-3):101561.
PMID: 39528363
The human brain undergoes rapid changes from the fetal stage to two years postnatally, during which proper structural and functional maturation lays the foundation for later cognitive and behavioral development....
5.
Neeman B, Sudhakar S, Biswas A, Rosenblum J, Sidpra J, DArco F, et al.
AJNR Am J Neuroradiol
. 2024 Aug;
45(10):1570-1577.
PMID: 39147584
Background And Purpose: Sotos syndrome is a rare autosomal dominant condition caused by pathogenic mutations in the gene that presents with craniofacial dysmorphism, overgrowth, seizures, and neurodevelopmental delay. Macrocephaly, ventriculomegaly,...
6.
Pogledic I, Mankad K, Severino M, Lerman-Sagie T, Jakab A, Hadi E, et al.
Brain
. 2024 Jul;
147(12):3982-4002.
PMID: 39054600
Brain malformations represent a heterogeneous group of abnormalities of neural morphogenesis, often associated with aberrations of neuronal connectivity and brain volume. Prenatal detection of brain malformations requires a clear understanding...
7.
Patel R, Park A, Marchi E, Gropman A, Whitehead M, Lyon G
Am J Med Genet A
. 2024 Jul;
194(12):e63821.
PMID: 39012200
NAA10-related (Ogden syndrome) and NAA15-related neurodevelopmental syndrome are known to present with varying degrees of intellectual disability, hypotonia, congenital cardiac abnormalities, seizures, and delayed speech and motor development. However, the...
8.
Patel R, Makwana R, Christ C, Marchi E, Ung N, Harpell R, et al.
medRxiv
. 2024 Jul;
PMID: 38978667
Background: -related (Ogden Syndrome) and -related neurodevelopmental syndromes present with varying degrees of intellectual disability, hypotonia, congenital cardiac abnormalities, seizures, and delayed speech and motor development. While there is much...
9.
Gebb J, Khalek N, Whitehead M, Oliver E
Magn Reson Imaging Clin N Am
. 2024 Jun;
32(3):513-528.
PMID: 38944438
Monochorionic twins are at risk for complications due to the presence of placental vascular anastomoses, including twin-twin transfusion syndrome, twin anemia-polycythemia sequence, selective fetal growth restriction, and twin reversed arterial...
10.
Simsek O, Manteghinejad A, Kotha A, Whitehead M
AJNR Am J Neuroradiol
. 2024 May;
45(9):1316-1321.
PMID: 38719610
Background And Purpose: In fetuses with lateral ventriculomegaly and normal posterior fossa cerebrospinal spaces, third ventricle distention is a compelling clue that supports a diagnosis of aqueductal stenosis. However, this...