نتائج البحث - "Hart G.W. Lidov"

1

Intracranial venous malformation masquerading as a meningioma in PI3KCA ‐related overgrowth spectrum disorder

المؤلفون: Alyaa Al-Ibraheemi, Siddharth Srivastava, Aristotelis Filippidis, Alfred P. See, Katie Pricola Fehnel, Hart G.W. Lidov, Darren B. Orbach

المصدر: American Journal of Medical Genetics Part A. 188:907-910

مصطلحات موضوعية: Pathology, medicine.medical_specialty, business.industry, medicine.disease, Discovery and development of mTOR inhibitors, Meningioma, PIK3CA gene, Glioma, Genetics, Medicine, Spectrum disorder, Lymphatic malformations, business, Venous malformation, neoplasms, Genetics (clinical), Superior sagittal sinus

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::681283591f3a7fc8b2b3a36dfc1dbab4Test
https://doi.org/10.1002/ajmg.a.62570Test

2

Spatiotemporal changes in diffusivity and anisotropy in fetal brain tractography

المؤلفون: Simon K. Warfield, Bahram Marami, Hart G.W. Lidov, Fedel Machado-Rivas, Camilo Jaimes, Onur Afacan, Ali Gholipour, Shadab Khan, Clemente Velasco-Annis

المصدر: Human Brain Mapping

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ef187a15a9c7a87b7fb9a9f2986bff4Test
https://doi.org/10.1002/hbm.25653Test

3

Medulloblastoma in the setting of megalencephaly polymicrogyria polydactyly hydrocephalus

المؤلفون: Lance H. Rodan, Hart G.W. Lidov, Muhamed Hadzipasic, Sanjay P. Prabhu, Heather E. Olson, Karen Wright, Madeline B Karsten, Katie Pricola Fehnel

المصدر: American Journal of Medical Genetics Part A. 185:1614-1618

مصطلحات موضوعية: Medulloblastoma, Polydactyly, business.industry, Infant, Anatomy, Fourth ventricle, medicine.disease, Hydrocephalus, Malformations of Cortical Development, Genetics, medicine, Polymicrogyria, Cyclin D2, Humans, Female, Genetic Predisposition to Disease, Megalencephaly, business, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35fffccea4be9fbb4b5a5bc23e3fd167Test
https://doi.org/10.1002/ajmg.a.62125Test

4

Loss of histone H3 trimethylation on lysine 27 and nuclear expression of transducin‐like enhancer 1 in primary intracranial sarcoma, DICER1 ‐mutant

المؤلفون: Hart G.W. Lidov, Sara O. Vargas, Keith L. Ligon, David Meredith, Mariangela Novello, Sanda Alexandrescu, Rita Alaggio

المصدر: Histopathology. 78:265-275

مصطلحات موضوعية: Male, Ribonuclease III, 0301 basic medicine, Pathology, medicine.medical_specialty, Histology, Adolescent, H3K27me3, CD99, DICER1 syndrome, DICER1, Pleuropulmonary blastoma, Biology, Methylation, Pathology and Forensic Medicine, DEAD-box RNA Helicases, Histones, 03 medical and health sciences, Histone H3, 0302 clinical medicine, Biomarkers, Tumor, medicine, Humans, Transducin, Child, Aged, Pineoblastoma, Glial fibrillary acidic protein, Brain Neoplasms, Lysine, primary intracranial sarcoma, TLE1, High-Throughput Nucleotide Sequencing, Infant, Sarcoma, General Medicine, medicine.disease, Immunohistochemistry, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation, biology.protein, Female, Immunostaining

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f77c62362c8d532132fd38efe45f8eaTest
https://doi.org/10.1111/his.14217Test

5

Somatic mutation involving diverse genes leads to a spectrum of focal cortical malformations

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::09d54f1a7b8a5e34586ff4179cebf388Test
https://doi.org/10.1101/2021.12.22.21267563Test

6

Increasing value of autopsies in patients with brain tumors in the molecular era

المؤلفون: Robert T. Jones, Pratiti Bandopadhayay, Hart G.W. Lidov, Peter E. Manley, Jared T. Ahrendsen, Kee Kiat Yeo, Sanda Alexandrescu, Mark W. Kieran, Susan N. Chi, Jessica Clymer, Mariella G. Filbin, Keith L. Ligon, Karen Wright

المصدر: Journal of Neuro-Oncology. 145:349-355

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1b250e49e1b74cae578379ef1617f50Test
https://doi.org/10.1007/s11060-019-03302-zTest

7

Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile

المساهمون: Graduate School, Pathology, APH - Aging & Later Life, APH - Mental Health, ANS - Cellular & Molecular Mechanisms, Clinical Genetics

المصدر: Modern pathology, 34(2), 264-279. Nature Publishing Group
Mod Pathol
Modern Pathology, 34(2), 264-279. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Somatic cell, Biology, Astrocytoma, Mechanistic Target of Rapamycin Complex 1, Tuberous Sclerosis Complex 1 Protein, Article, Pathology and Forensic Medicine, Ganglioglioma, Loss of heterozygosity, 03 medical and health sciences, Tuberous sclerosis, Young Adult, 0302 clinical medicine, Germline mutation, Mutation Rate, SDG 3 - Good Health and Well-being, Tuberous Sclerosis Complex 2 Protein, medicine, Subependymal zone, Humans, Child, Brain Neoplasms, Infant, Middle Aged, medicine.disease, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Child, Preschool, Female, TSC1, TSC2, Transcriptome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e2f51554e61f2c4bd5742fac222f16bTest
https://pure.amc.nl/en/publications/subependymal-giant-cell-astrocytomas-are-characterized-by-mtorc1-hyperactivation-a-very-low-somatic-mutation-rate-and-a-unique-gene-expression-profileTest(913c2a61-29c9-4a12-977d-44074f9b46ff).html

8

White matter mean diffusivity correlates with myelination in tuberous sclerosis complex

المؤلفون: Lana Vasung, Mustafa Sahin, Hart G.W. Lidov, Benoit Scherrer, Anna K. Prohl, Jolene M. Singh, Robbert R. Struyven, Onur Afacan, Jurriaan M. Peters, Joseph R. Madsen, Sanjay P. Prabhu, Simon K. Warfield, Maxime Taquet, Andrija Štajduhar, John J. Bushman

المصدر: Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1178-1190 (2019)
Annals of Clinical and Translational Neurology

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Neurosciences. Biological psychiatry. Neuropsychiatry, Luxol fast blue stain, White matter, 03 medical and health sciences, Tuberous sclerosis, 0302 clinical medicine, Nuclear magnetic resonance, Tuberous Sclerosis, Cortex (anatomy), Fractional anisotropy, medicine, Humans, Gliosis, RC346-429, Myelin Sheath, Research Articles, Cerebral Cortex, Neurons, business.industry, General Neuroscience, Infant, Newborn, Brain, Infant, medicine.disease, White Matter, Diffusion Tensor Imaging, 030104 developmental biology, medicine.anatomical_structure, Anisotropy, Female, Histopathology, Neurology. Diseases of the nervous system, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Research Article, RC321-571, Diffusion MRI

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0dd9d859c454010b97419545cc5aa4aTest
https://doi.org/10.1002/acn3.793Test

9

Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System

المؤلفون: Leslie Benson, Isaac H. Solomon, Hart G.W. Lidov, Lauren A. Henderson, Mark P. Gorman, Sanda Alexandrescu, Christine Duncan, Barbara A. Degar, Hojun Li

المصدر: Journal of Neuropathology & Experimental Neurology. 77:1079-1084

مصطلحات موضوعية: Central Nervous System, Pathology, medicine.medical_specialty, Systemic inflammation, Lymphohistiocytosis, Hemophagocytic, Pathology and Forensic Medicine, Diagnosis, Differential, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, medicine, Humans, UNC13D, Child, Histiocyte, Hemophagocytic lymphohistiocytosis, medicine.diagnostic_test, business.industry, Brain biopsy, Brain, General Medicine, Familial Hemophagocytic Lymphohistiocytosis, medicine.disease, Neurology, Child, Preschool, 030220 oncology & carcinogenesis, Brief Reports, Female, Neurology (clinical), Differential diagnosis, Hemophagocytosis, medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05716ec4dcd0c4e45abf071590a5c6b2Test
https://doi.org/10.1093/jnen/nly094Test

10

GEMC1-MCIDAS transcriptional program regulates multiciliogenesis in the choroid plexus and acts as a barrier to tumorigenesis

مصطلحات موضوعية: Ependymal Cell, Cerebrospinal fluid, Cilium, medicine, Cancer, Choroid plexus, Ventricular system, Biology, medicine.disease, Carcinogenesis, medicine.disease_cause, Hedgehog signaling pathway, Cell biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b677eadc9dfd5e8a704f66693cdef362Test
https://doi.org/10.1101/2020.11.22.393298Test

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