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Scholar Results 1 - 10 of about 101 related to NISHINO: Lupus erythematosus-like syndrome with selective complete deficiency of C1q. (0.07 sec) 

Lupus erythematosus-like syndrome with selective complete deficiency of C1q


H NISHINO, K SHIBUYA, Y NISHIDA, M … - Annals of Internal …, 1981 - Am Coll Physicians
A 37-year-old Japanese man in previously good health was hospitalized because of swelling of the
auricles and discoid erythema of the face. Clinical and laboratory findings satisfied the diagnostic
criteria for systemic lupus ...
Cited by 18 - Related articles - All 2 versions

A complete selective C1q deficiency in a patient with discoid lupus erythematosus ( …

- nih.gov [PDF] 
A Uenaka, T Akimoto, T Aoki, I … - Clinical and …, 1982 - pubmedcentral.nih.gov
A 32 year old male patient with discoid lupus erythematosus (DLE) was found to have a complete,
selective deficiency of Cl q subcomponent of the complement assessed either by haemolytic assay or
by protein determination. Addition ...
Cited by 8 - Related articles - All 2 versions

Clinical and immunological studies in a case of selective complete C1q deficiency

- nih.gov [PDF] 
AI Berkel, M Loos, Ö Sanal, G Mauff, Y … - Clinical and …, 1979 - pubmedcentral.nih.gov
SUMMARY A 10-year-old male with recurrent skin lesions and chronic infections was found to have a
selective deficiency of Clq after functional analysis of all complement components. The addition of
highly purified human Clq to the ...
Cited by 27 - Related articles - All 2 versions

A selective and complete absence of C1q in a patient with vasculitis and nephritis


JO Minta, CJ Winkler, WD Biggar, M Greenberg - Clinical Immunology and …, 1982 - Elsevier
An 8-year-old girl who has had a chronic rash with vasculitis involving her face and arms since the
first year of life was found to have a complete absence of the classical hemolytic complement and
functional C1 activity. All the ...
Cited by 8 - Related articles - All 2 versions

Familial C1q deficiency associated with renal and cutaneous disease.

- nih.gov [PDF] 
F Leyva-Cobian, I Moneo, F Mampaso, M … - Clinical and …, 1981 - pubmedcentral.nih.gov
A familial CIq deficiency of complement in three siblings has been established. The patients were
two brothers and a sister (12, 11 and 9 years old) with clinical and pathological features of
Rothmund-Thomson syndrome ...
Cited by 18 - Related articles - All 3 versions

[CITATION] A genetic defect of the C1q subcomponent of complement associated with …


RA Thompson, M Haeney, KB Reid, JG … - The New England …, 1980 - ncbi.nlm.nih.gov
1: N Engl J Med. 1980 Jul 3;303(1):22-4. A genetic defect of the C1q subcomponent of complement
associated with childhood (immune complex) nephritis. Thompson RA, Haeney M, Reid KB, Davies
JG, White RH, Cameron AH. Publication Types: Case Reports. ...
Cited by 31 - Related articles - All 2 versions

Selective C1q deficiency in a patient with systemic lupus erythematosus


T Orihara, K Tsuchiya, S Yamasaki, T Furuya - Br J Dermatol, 1987 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to display style sheets. In
this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the ...
Cited by 7 - Related articles - All 2 versions

Persistent Clq deficiency in a patient with a systemic lupus erythematosus-like …


DW Wara, EO Reiter, NE Doyle, H Gewurz, AJ … - The Journal of Pediatrics, 1975 - Elsevier
PF Koher and HJ Muller-Eberhard, Immunochemical quantitation of the third, fourth and fifth
components of human complement: Concentrations in the serum of healthy adults, J Immunol 99 (1967),
p. 1211. ... * Research supported ...
Cited by 21 - Related articles - All 3 versions

Selective complete Clq deficiency associated with systemic lupus erythematosus.


K Steinsson, RH McLean, M Merrow, NF … - The Journal of …, 1983 - ncbi.nlm.nih.gov
We report a case of systemic lupus erythematosus (SLE) and recurrent infections associated with
isolated Clq deficiency. A 17-year-old girl from Saudi Arabia was hospitalized with seizures, fever,
arthralgia, hair loss, oral ...
Cited by 15 - Related articles - All 2 versions

Characterization of a non-functional form of C1q found in patients with a genetically …


KB Reid, RA Thompson - Molecular immunology, 1983 - ncbi.nlm.nih.gov
A genetically defective form of C1q was purified from the sera of patients suffering from an immune
complex related disease and who were homozygous for the defect. The defective C1q was haemolytically
inactive and did not bind to immune ...
Cited by 15 - Related articles - All 2 versions


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