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492601 to 492700 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Association of specific overt behavior pattern with blood and cardiovascular findings; blood cholesterol level, blood clotting time, incidence of arcus senilis, and clinical coronary artery disease.
Fabry's disease: ocular findings in a female carrier. A light and electron microscopy study.
Carcinogenicity of dimethylnitrosamine in Swiss mice.
A method for the quantitative determination of neutral glycosphingolipids in urine sediment.
Urinary glycolipids in Fabry's disease. Their examination in the detection of atypical variants and the pre-symptomatic state.
Ocular pathology in fabry's disease. Histochemical and electron microscopic observations.
Glycolipid and mucopolysaccharide abnormality in fibroblasts of fabry's disease.
FAMILIAL ASPECTS OF DIFFUSE RENAL DISEASES.
Fabry's disease--glycolipid lipidosis. Histochemical and electron microscopic studies of two cases.
Angiokeratoma corporis diffusum universale (Fabry); first American report of a rare disorder.
Angiokeratoma corporis diffusum--Fabry's disease.
Peripheral nerve involvement in Fabry's disease.
Fabry's disease. Its ocular manifestations.
THE NEUROPATHOLOGY OF HEREDITARY DYSTOPIC LIPIDOSIS.
Exomphalos with macroglossia: a study of eleven cases.
Enzyme replacement in Fabry's disease, an inborn error of metabolism.
Angiokeratoma corporis diffusum. A clinical study of eight affected families.
Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.
RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia.
Oral mucosal lesions associated with betel quid, areca nut and tobacco chewing habits: consensus from a workshop held in Kuala Lumpur, Malaysia, November 25-27, 1996.
Lichenoid tissue reaction/interface dermatitis: clinical and histological perspectives.
Healing of oral lichenoid lesions after replacing amalgam restorations: a systematic review.
Genital lichen sclerosus (lichen sclerosus et atrophicus) in childhood and adolescence.
Drug-induced subacute cutaneous lupus erythematosus: a paradigm for bedside-to-bench patient-oriented translational clinical investigation.
Psoriasiform eruption induced by infliximab.
The possible premalignant character of oral lichen planus and oral lichenoid lesions: a prospective study.
Oral lichen planus: controversies surrounding malignant transformation.
Further evidence for Borrelia burgdorferi infection in morphea and lichen sclerosus et atrophicus confirmed by DNA amplification.
Classification, clinical manifestations, and immunopathological mechanisms of the epithelial variant of paraneoplastic autoimmune multiorgan syndrome: a reappraisal of paraneoplastic pemphigus.
Six area, six sign atopic dermatitis (SASSAD) severity score: a simple system for monitoring disease activity in atopic dermatitis.
Increased T-bet+ cytotoxic effectors and type I interferon-mediated processes in chronic graft-versus-host disease of the oral mucosa.
Gene expression of differentiation-specific keratins (K4, K13, K1 and K10) in oral non-dysplastic keratoses and lichen planus.
Rosana Santos Mota
Clinical validation and guidelines for the SCORAD index: consensus report of the European Task Force on Atopic Dermatitis.
T cell response to purified filtrate antigen 85 from Mycobacterium bovis Bacilli Calmette-Guérin (BCG) in leprosy patients.
Tumor necrosis factor promoter polymorphism and susceptibility to lepromatous leprosy.
Recombinant fusion protein identified by lepromatous sera mimics native Mycobacterium leprae in T-cell responses across the leprosy spectrum.
Prolonged treatment with recombinant interferon gamma induces erythema nodosum leprosum in lepromatous leprosy patients.
Analysis of cytokine production by Mycobacterium-reactive T cells. Failure to explain Mycobacterium leprae-specific nonresponsiveness of peripheral blood T cells from lepromatous leprosy patients.
Tumor necrosis factor production in patients with leprosy.
The influence of thalidomide on the clinical and immunologic manifestation of erythema nodosum leprosum.
Neutrophil Count Increased, Vietnamese
Clinical trial of pefloxacin and ofloxacin in the treatment of lepromatous leprosy.
MicroRNA-21 targets the vitamin D-dependent antimicrobial pathway in leprosy.
Novel responses of human skin to intradermal recombinant granulocyte/macrophage-colony-stimulating factor: Langerhans cell recruitment, keratinocyte growth, and enhanced wound healing.
CD1 expression by dendritic cells in human leprosy lesions: correlation with effective host immunity.
Type I interferon suppresses type II interferon-triggered human anti-mycobacterial responses.
T-cell release of granulysin contributes to host defense in leprosy.
Serum levels of tumour necrosis factor-alpha and interleukin-1 beta during leprosy reactional states.
Immunosuppressive roles for IL-10 and IL-4 in human infection. In vitro modulation of T cell responses in leprosy.
Detection of Toll-like receptor 2 (TLR2) mutation in the lepromatous leprosy patients.
Use of genetic profiling in leprosy to discriminate clinical forms of the disease.
IL-18 induction of IgE: dependence on CD4+ T cells, IL-4 and STAT6.
Cutting edge: a Toll-like receptor 2 polymorphism that is associated with lepromatous leprosy is unable to mediate mycobacterial signaling.
Pellagra in the United States: a historical perspective.
Nicotinamide: a double edged sword.
Acute pellagra during isoniazid therapy.
Effectiveness of food fortification in the United States: the case of pellagra.
Complications of midgut carcinoid tumors and carcinoid syndrome.
The major psychoses and neuroses as omega-3 essential fatty acid deficiency syndrome: substrate pellagra.
Leucine and pellagra.
Pellagra: A clue as to why energy failure causes diseases?
Pellagra among chronic alcoholics: clinical and pathological study of 20 necropsy cases.
Pellagra: dermatitis, dementia, and diarrhea.
Adverse effects of antituberculosis drugs.
DISORDERS OF AMINO-ACID TRANSPORT.
Biochemistry of tryptophan in health and disease.
The metabolic disorder in Hartnup disease.
Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features.
Nadirlene Pereira Gomes
Some aspects of copper metabolism in pellagra.
Autopsy of an Egyptian mummy.
The roentgen manifestations of thoracic actinomycosis.
Groin injuries in athletes.
Deficiency of interleukin-1 receptor antagonist responsive to anakinra.
CERVICAL VAGOTOMY FOR PULMONARY OSTEOARTHROPATHY.
Age, body composition, aerobic fitness and health condition as risk factors for musculoskeletal injuries in conscripts.
THE PATHOGENESIS OF ADJUVANT DISEASE IN THE RAT. I. A HISTOLOGIC STUDY OF EARLY LESIONS IN THE JOINTS AND SKIN.
Patterns of peripheral joint disease in ankylosing spondylitis.
HYPERTROPHIC PULMONARY OSTEOARTHROPATHY.
Overuse injuries in sports. A review.
Uncommon complications of early syphilis. Hepatitis, periostitis, iritis with papillitis, and meningitis.
The soleus syndrome. A cause of medial tibial stress (shin splints).
Incorporation of tenascin-C into the extracellular matrix by periostin underlies an extracellular meshwork architecture.
An analysis of spirochete load, strain, and pathology in a model of tick-transmitted Lyme borreliosis.
The biology of fracture healing in long bones.
Enchondroma versus chondrosarcoma in the appendicular skeleton: differentiating features.
Chondrosarcoma arising in osteochondroma.
Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions.
Assessment of interobserver variability and histologic parameters to improve reliability in classification and grading of central cartilaginous tumors.
Expression of connective tissue growth factor in cartilaginous tumors.
Reliability of histopathologic and radiologic grading of cartilaginous neoplasms in long bones.
Collagenase-3 (MMP-13) expression in chondrosarcoma cells and its regulation by basic fibroblast growth factor.
Synovial osteochondromatosis: a histopathological study of thirty cases.