Results 261 to 270 of about 31,605 (321)

Acute ataxia in children: etiological spectrum and clinical characteristics. [PDF]

Front Pediatr
Zhao Q, Gao C, Wang L, Liu C, Sun S, Li B.   +5 more
europepmc   +1 more source

Long-Term Disease-Free Survival Without Radiotherapy in a Pediatric Patient With Neurofibromatosis Type 1-Associated Medulloblastoma: A Case Report. [PDF]

Cureus
Ozono I, Yamasaki F, Onishi S, Yonezawa U, Horie N.   +4 more
europepmc   +1 more source

Rare Presentation of Homozygous S<i>LC20A2</i> Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature. [PDF]

Case Rep Genet
Baker L, Hadid F, Irshaidat SS, Altaraqji S, Benini R, Thabet F, Al Shami R, Kayyali H, Al Saleh R, Ben Omran T, Al Rayyahi J, El Beltagi A, Baha Juma, Ibrahim K.   +13 more
europepmc   +1 more source

Cerebellar neoplasms in children

Seminars in Roentgenology, 1990
EOPLASIA in children is uncommon; yet, the most common site for the occurrence of solid neoplasms in children is the central nervous system.’ The present incidence is approximately 2.5 central nervous system tumors per 100,000 children per year. Pediatric brain tumors, in fact, constitute 15% to 20% of all primary brain tumors.
Debra A. Gusnard
openaire   +3 more sources

Cerebellar T-cell lymphoma: an unusual primary intracranial neoplasm

Neuroradiology, 1992
Primary T-cell lymphoma within the central nervous system is extremely rare. Imaging characteristics appear indistinguishable from the more common B-cell lymphoma. A case of such a primary tumor is discussed and the MRI and CT findings presented.
J R, Knorr, R L, Ragland, B B, Stone, B A, Woda, N D, Gelber   +4 more
openaire   +3 more sources

Cortical cerebellar degeneration with testicular neoplasm

Acta Neuropathologica, 1985
Cortical cerebellar degeneration was found in a 28-year-old man with testicular neoplasm. The patient, who had undergone a left orchidectomy for the testicular tumor, developed progressive cerebellar symptoms with mental changes 7 months later. The autopsy revealed the spread of a malignant germ cell tumor of the testis, and cortical cerebellar ...
M, Yamada, R, Okeda, W, Chen, H, Nito, S, Hatakeyama, H, Tsukagoshi   +5 more
openaire   +3 more sources

Cerebellar neoplasm of mixed mesenchymal and neuroepithelial origin

Journal of Neurosurgery, 1983
✓ A 3½-year-old boy had a neoplasm of mixed mesenchymal and neuroepithelial origin in the cerebellar vermis. The tumor was composed of rhabdomyosarcoma and medulloblastoma. There was additional differentiation within the neuroepithelium, including neoplastic neurons, neuroblasts, astroglia, oligodendroglia, ependymal cells as well as foci of ...
S, Shuangshoti, S, O'Charoen
openaire   +3 more sources

Lhermitte-Duclos disease (dysplastic cerebellar gangliocytoma): a malformation, hamartoma or neoplasm?

Acta neurologica Scandinavica, 2002
Dysplastic gangliocytoma (Lhermitte-Duclos disease) is a rare disorder, characterized by a slowly progressive unilateral tumour mass of the cerebellar cortex. The fundamental nature of this apparently benign entity and in particular its pathogenesis remain unknown. The debate, whether it represents a neoplastic, malformative or hamartomatous lesion, is
D A, Nowak, H A, Trost
  +5 more sources