P E Neumann
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Explore the profile of P E Neumann including associated specialties, affiliations and a list of published articles.
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69
Citations
833
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Recent Articles
11.
Gershenfeld H, Neumann P, Li X, St Jean P, Paul S
J Neurosci
. 1999 May;
19(10):3731-8.
PMID: 10234005
To define the genetic contributions affecting individual differences in seizure threshold, a beta carboline [methyl-beta-carboline-3-carboxylate (beta-CCM)]-induced model of generalized seizures was genetically dissected in mice. beta-CCM is a GABAA receptor...
12.
Poderycki M, Simoes J, Todorova M, Neumann P, Seyfried T
J Neurogenet
. 1999 Apr;
12(2):67-86.
PMID: 10197158
The epileptic EL mouse has been studied extensively as a genetic model for idiopathic complex partial seizures in humans. The seizures in EL mice occur during routine handling at approximately...
13.
Greer W, Dobson M, Neumann P, Girouard G, Sparrow S, Riddell D
Genome
. 1998 Sep;
41(3):468-70.
PMID: 9729783
Previous reports concerning the location of D18S44 with respect to the centromere have been ambiguous. Also, it has not been possible, based on formerly reported markers, to show that contigs...
14.
Tremblay F, Gupta S, De Becker I, Guernsey D, Neumann P
Am J Ophthalmol
. 1998 Sep;
126(2):211-8.
PMID: 9727515
Purpose: To investigate the retinal function in aniridic patients with documented PAX6 mutations to determine the range of electroretinogram abnormalities in aniridic patients and to relate electroretinogram findings with specific...
15.
Gupta S, De Becker I, Tremblay F, Guernsey D, Neumann P
Am J Ophthalmol
. 1998 Sep;
126(2):203-10.
PMID: 9727514
Purpose: To detect and characterize mutations in cases of familial and sporadic aniridia in Maritime Canada, and to look for indications of genotype/phenotype correlation within the cohort. Methods: Twelve consecutive...
16.
Leong W, Schalkwyk L, Smallman D, Wong S, Storm D, Fine A, et al.
Nat Genet
. 1998 Jul;
19(3):289-91.
PMID: 9662407
The somatosensory (SI) cortex of mice displays a patterned, nonuniform distribution of neurons in layer IV called the 'barrelfield' (ref. 1). Thalamocortical afferents (TCAs) that terminate in layer IV are...
17.
Greer W, Riddell D, Gillan T, Girouard G, Sparrow S, Byers D, et al.
Am J Hum Genet
. 1998 Jun;
63(1):52-4.
PMID: 9634529
Niemann-Pick type D (NPD) disease is a progressive neurodegenerative disorder characterized by the accumulation of tissue cholesterol and sphingomyelin. This disorder is relatively common in southwestern Nova Scotia, because of...
18.
Gupta S, De Becker I, Guernsey D, Neumann P
Am J Ophthalmol
. 1998 Jun;
125(5):687-92.
PMID: 9625553
Purpose: Sporadic cases of aniridia have a 30% risk for the development of Wilms tumor. Current guidelines for sporadic aniridia recommend screening by renal ultrasonography for the presence of tumors...
19.
Gupta S, Hodge W, Damji K, Guernsey D, Neumann P
Am J Ophthalmol
. 1998 Apr;
125(4):547-9.
PMID: 9559741
Purpose: To identify the mutation responsible for lattice corneal dystrophy type 1 in an extended Canadian kindred. Methods: A search for a mutation in the candidate gene, kerato-epithelin, was carried...
20.
Neumann P, Mann O, Moss M, Schreiber W, Welch J, Langley G, et al.
Clin Biochem
. 1998 Feb;
30(8):607-12.
PMID: 9455613
Objectives: Acute intermittent porphyria (AIP) is caused by mutations in the porphobilinogen deaminase (PBGD) gene that disrupt the function of the enzyme. Many mutations that lead to decreased PBGD activity...