S Rosemberg
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Explore the profile of S Rosemberg including associated specialties, affiliations and a list of published articles.
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58
Citations
335
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Recent Articles
1.
Lima E, Otaduy M, Tsunemi M, Pincerato R, Cardoso E, Rosemberg S, et al.
AJNR Am J Neuroradiol
. 2012 Jul;
34(1):80-4.
PMID: 22766678
Background And Purpose: (1)H-MR spectroscopy is a useful tool in brain tumor evaluation. A critical point in obtaining representative spectra is the correct voxel positioning, which can be more accurate...
2.
Barbosa K, Oba-Shinjo S, Uno M, Carvalho P, Rosemberg S, Aguiar P, et al.
Int J Biol Markers
. 2008 Oct;
23(3):140-6.
PMID: 18949739
Epidermal growth factor receptor (EGFR) gene overexpression has been implicated in the development of many types of tumors, including glioblastomas, the most frequent diffusely infiltrating astrocytomas. However, little is known...
3.
Bhigjee A, Rosemberg S
Neurology
. 2006 Dec;
67(12 Suppl 4):S19-22.
PMID: 17190916
Worldwide, about 40 million people are living with HIV and 50 million people have neurocysticercosis (NCC). About 5% of patients with HIV and the majority of patients with NCC develop...
4.
Uno M, Oba-Shinjo S, Wakamatsu A, Huang N, Ferreira Alves V, Rosemberg S, et al.
Int J Biol Markers
. 2006 May;
21(1):50-7.
PMID: 16711514
Clarification of TP53 alterations is important to understand the mechanisms underlying the development of diffuse astrocytomas. It has been suggested that the alleles of TP53 at codon 72 differ in...
5.
Otaduy M, Leite C, Lacerda M, Costa M, Arita F, Prado E, et al.
AJNR Am J Neuroradiol
. 2006 Jan;
27(1):204-7.
PMID: 16418384
We describe how proton MR spectroscopy ((1)H-MR spectroscopy) was useful in elucidating the diagnosis of galactosemia in an undiagnosed 6-month-old infant. In vivo (1)H-MR spectroscopy of the brain showed a...
6.
Nagae-Poetscher L, Bibat G, Philippart M, Rosemberg S, Fatemi A, Lacerda M, et al.
Neurology
. 2004 Apr;
62(7):1206-9.
PMID: 15079028
We describe three cases of the rare syndrome of leukoencephalopathy, brain calcifications, and cysts. Conventional MRI, proton spectroscopy, and diffusion-weighted imaging yielded additional information on the disease. Imaging findings favor...
7.
Suzuki O, Sertie A, Der Kaloustian V, Kok F, Carpenter M, Murray J, et al.
Am J Hum Genet
. 2002 Nov;
71(6):1320-9.
PMID: 12415512
Knobloch syndrome (KS) is a rare disease characterized by severe ocular alterations, including vitreoretinal degeneration associated with retinal detachment and occipital scalp defect. The responsible gene, COL18A1, has been mapped...
8.
Albano L, Zatz M, Kim C, Bertola D, Sugayama S, Kok F, et al.
Rev Hosp Clin Fac Med Sao Paulo
. 2002 Jan;
56(5):143-8.
PMID: 11781594
Introduction: Friedreich's ataxia is a neurodegenerative disorder whose clinical diagnostic criteria for typical cases basically include: a) early age of onset (< 20 or 25 years), b) autosomal recessive inheritance,...
9.
Kosel S, Grasbon-Frodl E, Arima K, Chimelli L, Hahn M, Hashizume Y, et al.
Neurogenetics
. 2001 Aug;
3(3):163-70.
PMID: 11523568
DNA extracted from formalin-fixed and paraffin-embedded brain tissue is known to contain as yet ill-characterized inhibitors of the PCR process. As part of a project that aims to clarify the...
10.
Nitrini R, Teixeira da Silva L, Rosemberg S, Caramelli P, Carrilho P, Iughetti P, et al.
Arq Neuropsiquiatr
. 2001 Jun;
59(2-A):161-4.
PMID: 11400017
Objective: To compare the clinical features of a familial prion disease with those of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Background: Prion diseases are not usually considered...