M L Schroeder
Overview
Explore the profile of M L Schroeder including associated specialties, affiliations and a list of published articles.
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69
Citations
523
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Recent Articles
1.
Jilkina O, Thompson J, Kwan L, Van Caeseele P, Rockman-Greenberg C, Schroeder M
Mol Genet Metab Rep
. 2016 Nov;
1:324-333.
PMID: 27896105
In Manitoba, Canada, the overall incidence of Severe Combined Immunodeficiency (SCID) is three-fold higher than the national average, with SCID overrepresented in two population groups: Mennonites and First Nations of...
2.
Schroeder M, Triggs-Raine B, Zelinski T
BMC Med Genet
. 2016 Jul;
17(1):50.
PMID: 27448562
Background: Primary immunodeficiency is a life-threatening genetic disease that appeared to have an increased incidence in Manitoba Mennonites. Determining the genetic basis of this immunodeficiency was an essential step for...
3.
Schroeder M, Rayner H
Can Fam Physician
. 2011 Feb;
30:1803-6.
PMID: 21279095
Blood transfusion therapy carries a small risk of complications-usually minor-which include allergic reactions, hemolysis, and the transmission of infections. Fatal hemolytic transfusion reactions are rare and are usually due to...
4.
5.
Yang K, Schroeder M, Cherng J, Lin P
Eur J Immunogenet
. 2003 Aug;
30(4):283-7.
PMID: 12919290
In a routine HLA antibody screening cross-match test using the complement-mediated lymphocytotoxicity (LCT) assay, we discovered an antibody, in a transfused Caucasian woman, recognizing an Oriental restricted antigen that does...
6.
Wiseman M, Orr P, MacDonald S, Schroeder M, Toole J
J Am Acad Dermatol
. 2001 May;
44(6):952-6.
PMID: 11369906
Background: Actinic prurigo (AP) is an idiopathic familial photodermatitis. AP of the Inuit is rarely reported and poorly characterized. Objective: Our purpose was to examine the clinical features and HLA...
7.
Villa A, Sobacchi C, Notarangelo L, Bozzi F, Abinun M, Abrahamsen T, et al.
Blood
. 2001 Jan;
97(1):81-8.
PMID: 11133745
Severe combined immunodeficiency (SCID) comprises a heterogeneous group of primary immunodeficiencies, a proportion of which are due to mutations in either of the 2 recombination activating genes (RAG)-1 and -2,...
8.
Goldner E, Srikameswaran S, Schroeder M, Livesley W, Birmingham C
Psychiatry Res
. 1999 Apr;
85(2):151-9.
PMID: 10220006
This study examined patients with eating disorders on personality pathology using a dimensional method. Female subjects who met DSM-IV diagnostic criteria for eating disorder (n = 136) were evaluated and...
9.
Johnson S, Schroeder M, Sanchez J, Kirk M
J Comp Neurol
. 1999 Apr;
406(4):476-86.
PMID: 10205024
Rhythmic biting, a component of consummatory feeding behavior in the sea hare Aplysia californica, is eliminated following bilateral cerebral-buccal connective (CBC) crushes and recovers within 14 days postlesion. To assess...
10.
Laitinen A, Hietala M, Haworth J, Schroeder M, Seargeant L, Greenberg C, et al.
Clin Genet
. 1997 Mar;
51(3):174-8.
PMID: 9137882
Aspartylglucosaminuria (AGU) is a lysosomal storage disease caused by deficiency of aspartylglucosaminidase. The disease is overrepresented in the Finnish population, in which one missense mutation (Cys163Ser) is responsible for 98%...