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483101 to 483200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
An experimental study of the etiology of rum fits and delirium tremens.
Genetic predisposition to organ-specific endpoints of alcoholism.
Ethanol withdrawal in mice bred to be genetically prone or resistant to ethanol withdrawal seizures.
The glutamatergic basis of human alcoholism.
Chest Pain, Flushing, hypertension
Multiple withdrawals from chronic ethanol "kindles" inferior collicular seizure activity: evidence for kindling of seizures associated with alcoholism.
Altered NMDA glutamate receptor antagonist response in individuals with a family vulnerability to alcoholism.
Utilising survey data to inform public policy: comparison of the cost-effectiveness of treatment of ten mental disorders.
Heterotopic ossification: a review.
Hematopoietic stem-cell contribution to ectopic skeletogenesis.
Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients.
The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients.
In vivo somatic cell gene transfer of an engineered Noggin mutein prevents BMP4-induced heterotopic ossification.
Fibrodysplasia ossificans progressiva.
Transgenic mice overexpressing BMP4 develop a fibrodysplasia ossificans progressiva (FOP)-like phenotype.
Inherited human diseases of heterotopic bone formation.
Dysregulated BMP signaling and enhanced osteogenic differentiation of connective tissue progenitor cells from patients with fibrodysplasia ossificans progressiva (FOP).
Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva.
The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization.
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.
Constitutively activated ALK2 and increased SMAD1/5 cooperatively induce bone morphogenetic protein signaling in fibrodysplasia ossificans progressiva.
Conversion of vascular endothelial cells into multipotent stem-like cells.
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
Fatal enterovirus 71 encephalomyelitis.
Basis of neurovirulence in Sindbis virus encephalomyelitis of mice.
Clinical features and risk factors of pulmonary oedema after enterovirus-71-related hand, foot, and mouth disease.
A new coronavirus-like particle associated with diarrhea in swine.
Chronic enterovirus infection in patients with postviral fatigue syndrome.
The T cell chemoattractant IFN-inducible protein 10 is essential in host defense against viral-induced neurologic disease.
Anatomical substrates for the central control of sympathetic outflow to interscapular adipose tissue during cold exposure.
Chronic arthritis in goats caused by a retrovirus.
Darkened skin pigmentation, hepatomegaly, xantthelasma
Para-infectious encephalomyelitis and related syndromes; a critical review of the neurological complications of certain specific fevers.
Treatment of experimental encephalomyelitis with a peptide analogue of myelin basic protein.
Persistent infection of oligodendrocytes in Theiler's virus-induced encephalomyelitis.
High incidence of spontaneous autoimmune encephalomyelitis in immunodeficient anti-myelin basic protein T cell receptor transgenic mice.
Anti-IL-23 therapy inhibits multiple inflammatory pathways and ameliorates autoimmune encephalomyelitis.
Appreciation of metaphoric alternative word meanings by left and right brain-damaged patients.
Aphasia after stroke: natural history and associated deficits.
Progressive language disorder due to lobar atrophy.
Conduction aphasia and the arcuate fasciculus: A reexamination of the Wernicke-Geschwind model.
Naming in semantic dementia--what matters?
Functional MRI follow-up study of language processes in healthy subjects and during recovery in a case of aphasia.
Brain plasticity in poststroke aphasia: what is the contribution of the right hemisphere?
Verbal and design fluency in patients with frontal lobe lesions.
A meta-analytic review of verbal fluency performance following focal cortical lesions.
Asymbolia for pain: a sensory-limbic disconnection syndrome.
Hypoperfusion of Wernicke's area predicts severity of semantic deficit in acute stroke.
The anatomical basis of conduction aphasia.
Training-induced brain plasticity in aphasia.
Plasticity of language-related brain function during recovery from stroke.
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome.
Cancer predisposition caused by elevated mitotic recombination in Bloom mice.
BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates.
Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity.
The Bloom's syndrome gene product interacts with topoisomerase III.
Bloom syndrome: a mendelian prototype of somatic mutational disease.
The Bloom's syndrome helicase unwinds G4 DNA.
Mechanism of homologous recombination: mediators and helicases take on regulatory functions.
The Bloom's syndrome gene product promotes branch migration of holliday junctions.
The Bloom's syndrome gene product is homologous to RecQ helicases.
The Bloom's syndrome helicase suppresses crossing over during homologous recombination.
Inflammatory cytokines in the tears of patients with ocular rosacea.
A clinical trial of tetracycline in rosacea.
Small-intestinal mucosal abnormalities in various skin diseases--fact or fancy?
Meibomian gland secretion in the red eyes of rosacea.
Blepharitis: current strategies for diagnosis and management.
Whole genome comparisons of Fragaria, Prunus and Malus reveal different modes of evolution between Rosaceous subfamilies.
Rosacea: II. Therapy.
Minocycline effect on meibomian gland lipids in meibomianitis patients.
Andrew C Nyborg
Clinical practice. Rosacea.
Flow cytometric analysis of conjunctival epithelium in ocular rosacea and keratoconjunctivitis sicca.
The cell cycle time in the flat (avillous) mucosa of the human small intestine.
Standard classification of rosacea: Report of the National Rosacea Society Expert Committee on the Classification and Staging of Rosacea.
Regulation of MMP-9 activity in human tear fluid and corneal epithelial culture supernatant.
Antimicrobial peptides and the skin immune defense system.
Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea.
Letter: Sexual transmission of intestinal parasites.
Idiopathic perianal pruritus: washing compared with topical corticosteroids.
Clinical use of micronized purified flavonoid fraction for treatment of symptoms after hemorrhoidectomy: results of a randomized, controlled, clinical trial.
Abnormal transient internal sphincter relaxation in idiopathic pruritus ani: physiological evidence from ambulatory monitoring.
What every gastroenterologist needs to know about common anorectal disorders.
Physiological study of pruritus ani.
Perianal Paget's disease. Classification and review of management: report of two cases.
Common superficial fungal infections in patients with AIDS.
Capsaicin and menthol in the treatment of itch and pain: recently cloned receptors provide the key.
Treatment of intractable pruritus ani.
Prospective studies on the etiology and treatment of pruritus ani.
Primary care office management of perianal and anal disease.
ABC of colorectal diseases. Pruritus ani.
Pruritus ani. Causes and concerns.
M Celeste Ferreira-Cornwell
Intradermal methylene blue injection for the treatment of intractable idiopathic pruritus ani.
Intradermal methylene blue injection for the treatment of intractable idiopathic pruritus ani: results of 30 cases.