R L Schelper
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Explore the profile of R L Schelper including associated specialties, affiliations and a list of published articles.
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44
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449
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Recent Articles
1.
Mathews K, Mills K, Bailey H, Schelper R, Murray J
Muscle Nerve Suppl
. 2013 Apr;
(2):S98-102.
PMID: 23573594
Myodystrophy (myd) is an autosomal-recessive mouse mutation with dystrophic skeletal muscle. We propose that myd may be a model of the human disorder facioscapulohumeral dystrophy (FSHD) on the basis of...
2.
Lieberman K, Fuller C, Caruso R, Schelper R
Neuroradiology
. 2001 Aug;
43(7):555-8.
PMID: 11512585
A 49-year-old man developed a gliosarcoma with prominent osteoid components 15 months after surgical resection and postoperative radiation and chemotherapy for a right frontal glioblastoma multiforme. The recurrent tumor was...
3.
Nanni L, Schelper R, Muenke M
Front Biosci
. 2000 Mar;
5:D334-42.
PMID: 10704430
Holoprosencephaly (HPE) is a common developmental defect of the human forebrain and midface. Pathological studies have identified different categories of severity of the brain and craniofacial malformations observed in HPE,...
4.
Davis B, Reed L, Schelper R
Eur Neurol
. 1998 Sep;
40(3):141-5.
PMID: 9748671
We present updated information on a previously reported kindred with an autosomal dominant disorder variably expressed as indifference to pain, dementia, and ataxia. Additional clinical and radiological information is presented,...
5.
Reed L, Schmidt M, Wszolek Z, Balin B, Soontornniyomkij V, Lee V, et al.
J Neuropathol Exp Neurol
. 1998 Jun;
57(6):588-601.
PMID: 9630238
A group of similar autosomal dominant hereditary neurodegenerative disorders have been linked to chromosome 17 in thirteen kindreds. One of these disorders, known as pallido-ponto-nigral degeneration (PPND), is characterized by...
6.
Reed L, Grabowski T, Schmidt M, Morris J, Goate A, Solodkin A, et al.
Ann Neurol
. 1997 Oct;
42(4):564-72.
PMID: 9382467
Several familial dementing conditions with atypical features have been characterized, but only rarely is the neuropathology dominated solely by neurofibrillary lesions. We present a Midwestern American pedigree spanning four generations...
7.
Kuljis R, Schelper R
J Neuropathol Exp Neurol
. 1996 Jan;
55(1):25-35.
PMID: 8558169
Cognitive impairment in the absence of lesions indicative of Alzheimer's disease and other dementing conditions has long been recognized in a subgroup of patients with motor neuron disease MND), including...
8.
Mathews K, Rapisarda D, Bailey H, Murray J, Schelper R, Smith R
J Neuropathol Exp Neurol
. 1995 Jul;
54(4):601-6.
PMID: 7602333
Facioscapulohumeral dystrophy (FSHD) is an autosomal dominant disease of unknown pathogenesis which is characterized by weakness of the face and shoulder girdle. It is associated with a sensorineural hearing loss...
9.
Mills K, Mathews K, Schelper R, Schmalzel R, Bailey H, Nadeau J, et al.
Mamm Genome
. 1995 Apr;
6(4):278-80.
PMID: 7613034
Myodystrophy (myd), an autosomal recessive mutation of the mouse characterized by progressive weakness and dystrophic muscle histology, maps to the central portion of Chromosome (Chr) 8 (Lane et al. J....
10.
Hemalatha S, Kerr D, Wexler I, Lusk M, Kaung M, Du Y, et al.
Hum Mol Genet
. 1995 Feb;
4(2):315-8.
PMID: 7757088
No abstract available.