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Challenges and opportunities facing medical education

Transactions of the American Clinical and Climatological Association, 2011, Vol.122, p.48-58

Densen, Peter

2011

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James A. Clifton, III, MD 1923-2014

Transactions of the American Clinical and Climatological Association, 2015, Vol.126, p.lxxxviii-xci

Densen, Peter

2015

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A Point Mutation Creating a 3' Splice Site in C8A Is a Predominant Cause of C8α-γ Deficiency in African Americans

The Journal of immunology (1950), 2020-09, Vol.205 (6), p.1535-1539

2020

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The complement system in pediatric systemic lupus erythematosus, atypical hemolytic uremic syndrome, and complocentric membranoglomerulopathies

Current opinion in rheumatology, 2012-09, Vol.24 (5), p.522-529

2012

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Autoantibody stabilization of the classical pathway C3 convertase leading to C3 deficiency and Neisserial sepsis: C4 nephritic factor revisited

Clinical immunology (Orlando, Fla.), 2012-12, Vol.145 (3), p.241-250

2012

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Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome: emerging insights for vascular integrity

Current infectious disease reports, 2005-09, Vol.7 (5), p.319-321

Densen, Peter

2005

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University of Iowa Carver College of Medicine

Academic medicine, 2010-09, Vol.85 (9 Suppl), p.S228-S232

2010

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Lipooligosaccharide Pk(Galα1-4Galβ1-4Glc) Epitope of Moraxella catarrhalis Is a Factor in Resistance to Bactericidal Activity Mediated by Normal Human Serum

Infection and Immunity, 2000-09, Vol.68 (9), p.5261-5268

2000

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A 9-year-old boy with chronic urticaria and progressive spondyloarthritis

Allergy and asthma proceedings, 2013-01, Vol.34 (1), p.103-107

2013

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COMPLEMENT DEFICIENCIES AND MENINGOCOCCAL DISEASE

Clinical and experimental immunology, 1991-10, Vol.86 (Supplement_1), p.57-62

Densen, Peter

1991

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Type II Human Complement C2 Deficiency

The Journal of biological chemistry, 1996-03, Vol.271 (10), p.5824-5831

1996

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Lipooligosaccharide P k (Galα1-4Galβ1-4Glc) Epitope of Moraxella catarrhalis Is a Factor in Resistance to Bactericidal Activity Mediated by Normal Human Serum

Infection and immunity, 2000-09, Vol.68 (9), p.5261-5268

2000

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Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency

Journal of clinical immunology, 2003-07, Vol.23 (4), p.297-305

2003

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Complement deficiency states and meningococcal disease

Immunologic research, 1993-01, Vol.12 (3), p.295-311

1993

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Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing

The Journal of biological chemistry, 1992-05, Vol.267 (13), p.9347-9353

1992

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Antineutrophil antibodies in infectious mononucleosis

The American journal of medicine, 1984, Vol.76 (1), p.85-90

1984

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Teaching a screening musculoskeletal examination: a randomized, controlled trial of different instructional methods

Academic medicine, 1999-02, Vol.74 (2), p.199-201

1999

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Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretion

The Journal of biological chemistry, 1996-03, Vol.271 (10), p.5824-5831

1996

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Delineation of additional genetic bases for C8 beta deficiency. Prevalence of null alleles and predominance of C-->T transition in their genesis

The Journal of immunology (1950), 1995-11, Vol.155 (10), p.5022-5028

1995

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Killing of Neisseria meningitidis by human neutrophils: implications for normal and complement-deficient individuals

The Journal of infectious diseases, 1987-06, Vol.155 (6), p.1266-1275

1987

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Plasma tumor necrosis factor levels in patients with presumed sepsis. Results in those treated with antilipid A antibody vs placebo

JAMA : the journal of the American Medical Association, 1989-07, Vol.262 (2), p.249

1989

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Familial Properdin Deficiency and Fatal Meningococcemia

The New England journal of medicine, 1987-04, Vol.316 (15), p.922-926

1987

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Invasive Haemophilus influenzae type b infection in a child with familial deficiency of the beta subunit of the eighth component of complement

The Journal of pediatrics, 1996, Vol.128 (1), p.102-103

1996

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A teaching rotation for residents

Academic medicine, 1994-05, Vol.69 (5), p.434-434

1994

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Mechanisms of Contraction Induced by Human Leukocytes in Normal and Atherosclerotic Arteries

Circulation research, 1991-09, Vol.69 (3), p.871-880

1991

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Challenges and opportunities facing medical education

James A. Clifton, III, MD 1923-2014

A Point Mutation Creating a 3' Splice Site in C8A Is a Predominant Cause of C8α-γ Deficiency in African Americans

The complement system in pediatric systemic lupus erythematosus, atypical hemolytic uremic syndrome, and complocentric membranoglomerulopathies

Autoantibody stabilization of the classical pathway C3 convertase leading to C3 deficiency and Neisserial sepsis: C4 nephritic factor revisited

Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome: emerging insights for vascular integrity

University of Iowa Carver College of Medicine

Lipooligosaccharide Pk(Galα1-4Galβ1-4Glc) Epitope of Moraxella catarrhalis Is a Factor in Resistance to Bactericidal Activity Mediated by Normal Human Serum

A 9-year-old boy with chronic urticaria and progressive spondyloarthritis

COMPLEMENT DEFICIENCIES AND MENINGOCOCCAL DISEASE

Type II Human Complement C2 Deficiency

Lipooligosaccharide P k (Galα1-4Galβ1-4Glc) Epitope of Moraxella catarrhalis Is a Factor in Resistance to Bactericidal Activity Mediated by Normal Human Serum

Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency

Complement deficiency states and meningococcal disease

Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing

Antineutrophil antibodies in infectious mononucleosis

Teaching a screening musculoskeletal examination: a randomized, controlled trial of different instructional methods

Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretion

Delineation of additional genetic bases for C8 beta deficiency. Prevalence of null alleles and predominance of C-->T transition in their genesis

Killing of Neisseria meningitidis by human neutrophils: implications for normal and complement-deficient individuals

Plasma tumor necrosis factor levels in patients with presumed sepsis. Results in those treated with antilipid A antibody vs placebo

Familial Properdin Deficiency and Fatal Meningococcemia

Invasive Haemophilus influenzae type b infection in a child with familial deficiency of the beta subunit of the eighth component of complement

A teaching rotation for residents

Mechanisms of Contraction Induced by Human Leukocytes in Normal and Atherosclerotic Arteries

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