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431601 to 431700 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Leukemia inhibitory factor regulates glucocorticoid receptor expression in the hypothalamic-pituitary-adrenal axis.
Opposing effects of pituitary leukemia inhibitory factor and SOCS-3 on the ACTH axis response to inflammation.
Leukemia inhibitory factor signaling is implicated in embrionic development of the HPA axis.
Progesterone decreases levels of the adhesion protein E-cadherin and promotes invasiveness of steroid receptor positive breast cancers.
Progesterone stimulates proliferation and promotes cytoplasmic localization of the cell cycle inhibitor p27 in steroid receptor positive breast cancers.
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Non-animal Replacements for Acute Toxicity Testing.
Sexually transmitted infection clinics as safety net providers: exploring the role of categorical sexually transmitted infection clinics in an era of health care reform.
Nebulized epinephrine for croup in children.
Tracheostomy in children: a population-based experience over 17 years.
Congenital central hypoventilation syndrome; safety of early transition to non-invasive ventilation.
Delayed diagnosis of high proximal tracheoesophageal fistula in esophageal atresia and a novel approach to the treatment of tracheomalacia by submanubrial tracheopexy.
Inconclusive diagnosis of cystic fibrosis after newborn screening.
The legal aspects of expedited partner therapy practice: do state laws and policies really matter?
Gonorrhea treatment practices in the STD Surveillance Network, 2010-2012.
Neighborhoods at risk: estimating risk of higher Neisseria gonorrhoeae incidence among women at the census tract level.
Children with special health care needs program: urban/rural comparisons.
Early intervention for childhood anxiety in a school setting: outcomes for an economically disadvantaged population.
Glycogen Storage Disease Type VIII
A review of surgical intervention in the setting of traumatic central cord syndrome.
Diagnostic criteria of traumatic central cord syndrome. Part 3: descriptive analyses of neurological and functional outcomes in a prospective cohort of traumatic motor incomplete tetraplegics.
Acute central cord syndrome: injury mechanisms and stress features.
A novel classification system for traumatic central cord syndrome: the central cord injury scale (CCIS).
The urgency of surgical decompression in acute central cord injuries with spondylosis and without instability.
The long-term outcome after central cord syndrome: a study of the natural history.
A histopathological analysis of the human cervical spinal cord in patients with acute traumatic central cord syndrome.
Current practice in the timing of surgical intervention in spinal cord injury.
Injury to the spinal cord without radiological abnormality (SCIWORA) in adults.
A child with progressive multiple tracheal diverticulae: a variation of the Mounier-Kuhn syndrome.
[Case report: respiratory infection due to Alcaligenes xylosoxidans in a patient with Mounier-Kuhn syndrome].
Tracheal side effects following fetal endoscopic tracheal occlusion for severe congenital diaphragmatic hernia.
A man with a large trachea.
[Congenital megatrachea and bronchiectasis (Mounier-Kuhn syndrome)].
Respiratory failure due to tracheobronchomalacia.
Mounier-Kuhn syndrome: report of 8 cases of tracheobronchomegaly with associated complications.
Commentary: yet more to see down the bronchial tree?
A 74-year-old man with memory loss and neuropathy who enjoys alcoholic beverages.
Involvement of microglia in the ethanol-induced neuropathic pain-like state in the rat.
Painful alcoholic polyneuropathy with predominant small-fiber loss and normal thiamine status.
Alcoholic neuropathy: possible mechanisms and future treatment possibilities.
Alcohol consumption enhances antiretroviral painful peripheral neuropathy by mitochondrial mechanisms.
Mechanically-evoked C-fiber activity in painful alcohol and AIDS therapy neuropathy in the rat.
Peripheral nerve conduction abnormalities in children exposed to alcohol in utero.
Peripheral nerve size in normals and patients with polyneuropathy: an ultrasound study.
Muscle pain in models of chemotherapy-induced and alcohol-induced peripheral neuropathy.
Alcohol-induced stress in painful alcoholic neuropathy.
Neurocognitive impairment associated with alcohol use disorders: implications for treatment.
[Differential diagnosis of glycogenoses].
[Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
[Clinico-biochemical and morphological characteristics of the hepatic form of glycogenosis in children].
Use of platelets, mononuclear and polymorphonuclear cells in the diagnosis of glycogen storage disease type VI.
The behavior of hepatic phosphorylase b kinase, phosphorylase a and b after administration of glucagon to patients with glycogen storage disease type VIa.
Radiography of glycogen storage diseases.
Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VI.
A novel mutation (G233D) in the glycogen phosphorylase gene in a patient with hepatic glycogen storage disease and residual enzyme activity.
The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.
Inflammatory papillary stenosis due to Giardia lamblia in a patient with hyper-immunoglobulin M immunodeficiency syndrome.
Clinical and genetic analysis of patients with X-linked hyper-IgM syndrome.
CD40 ligand deficiency: neurologic sequelae with radiographic correlation.
Analysis of genetic defects in patients with the common variable immunodeficiency phenotype in a single Taiwanese tertiary care hospital.
Impaired maintenance of naturally acquired T-cell memory to the meningococcus in patients with B-cell immunodeficiency.
Poorly differentiated gastroenteropancreatic neuroendocrine carcinoma associated with X-linked hyperimmunoglobulin M syndrome.
Expanding the clinical and genetic spectrum of human CD40L deficiency: the occurrence of paracoccidioidomycosis and other unusual infections in Brazilian patients.
Partial immune reconstitution of X-linked hyper IgM syndrome with recombinant CD40 ligand.
Assessment and clinical interpretation of reduced IgG values.
Toll-like receptor 7-induced naive human B-cell differentiation and immunoglobulin production.
Analysis of somatic hypermutation in X-linked hyper-IgM syndrome shows specific deficiencies in mutational targeting.
Dendritic Cell Sarcoma, Interdigitating
Feline parvovirus propagates in cat bone marrow cultures and inhibits hematopoietic colony formation in vitro.
Characterisation of a protective linear B cell epitope against feline parvoviruses.
Serosurvey for selected virus infections of wild carnivores in Taiwan and Vietnam.
Comparison of feline parvovirus subspecific strains using monoclonal antibodies against a feline panleukopenia virus.
Pathogenic potential of canine parvovirus types 2a and 2c in domestic cats.
Characteristics of feline panleucopaenia virus strains enabling definitive classification as parvoviruses.
Response of mink, skunk, red fox and raccoon to inoculation with mink virus enteritis, feline panleukopenia and canine parvovirus and prevalence of antibody to parvovirus in wild carnivores in Ontario.
Viral infections in free-living populations of the European wildcat.
An enteric disease of dogs reselmbing feline panleucopaenia.
Differentiation of Haemobartonella canis and Mycoplasma haemofelis on the basis of comparative analysis of gene sequences.
Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever.
Two monoclonal antibodies with defined epitopes of P44 major surface proteins neutralize Anaplasma phagocytophilum by distinct mechanisms.
Prevalence of Bartonella species, haemoplasma species, Ehrlichia species, Anaplasma phagocytophilum, and Neorickettsia risticii DNA in the blood of cats and their fleas in the United States.
Development and evaluation of a PCR-based assay for detection of Haemobartonella felis in cats and differentiation of H. felis from related bacteria by restriction fragment length polymorphism analysis.
Candidatus Neoehrlichia mikurensis infection identified in 2 hematooncologic patients: benefit of molecular techniques for rare pathogen detection.
Ultrastructure and phylogenetic analysis of 'Candidatus Neoehrlichia mikurensis' in the family Anaplasmataceae, isolated from wild rats and found in Ixodes ovatus ticks.
Blurred Vision, Large Cisterna Magna, alcohol consumption, nystagmus, cerebellar sign, tinnitus
Blurred Vision, Large Cisterna Magna, alcohol consumption, nystagmus, cerebellar sign
Defective, Irregular Tarsal Ossification
Blurred Vision, Large Cisterna Magna, alcohol consumption, nystagmus
Restricted Joint Mobility (Shoulders, Elbows, Hips)
Cortols : Cortolone Ratio Low
Blurred Vision, Large Cisterna Magna, alcohol consumption
Diagnosis of fructose-1,6-bisphosphatase deficiency using leukocytes: normal leukocyte enzyme activity in three female patients.
Deficiency of glucose-6-phosphate dehydrogenase found in a case of hepatic fructose-1,6-diphosphatase deficiency.