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485501 to 485600 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.
Inaccuracy of the International Classification of Diseases (ICD-9-CM) in identifying the diagnosis of ischemic cerebrovascular disease.
Deglycosylated anti-amyloid-beta antibodies eliminate cognitive deficits and reduce parenchymal amyloid with minimal vascular consequences in aged amyloid precursor protein transgenic mice.
PROACT: a phase II randomized trial of recombinant pro-urokinase by direct arterial delivery in acute middle cerebral artery stroke. PROACT Investigators. Prolyse in Acute Cerebral Thromboembolism.
Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain.
Gender-linked brain injury in experimental stroke.
Presence and extent of severe facet joint osteoarthritis are associated with back pain in older adults.
Comparison of minimally invasive fusion and instrumentation versus open surgery for severe stenotic spondylolisthesis with high-grade facet joint osteoarthritis.
Association of HTRA1 promoter polymorphism with spinal disc degeneration in Japanese women.
Surgical treatment for atlantooccipital osteoarthritis: a case report of two patients.
Association between disc degeneration and degenerative spondylolisthesis? Pilot study.
Low back pain and lumbar spine osteoarthritis: how are they related?
Longitudinal study of radiographic spinal osteoarthritis in a macaque model.
Does lumbar spinal degeneration begin with the anterior structures? A study of the observed epidemiology in a community-based population.
Diagnosing axial spondyloarthropathy. The new Assessment in SpondyloArthritis international Society criteria: MRI entering centre stage.
Association between age, sex, BMI and CT-evaluated spinal degeneration features.
Prevalence of concurrent lumbar and cervical arthrosis: an anatomic study of cadaveric specimens.
In vivo topographic analysis of lumbar facet joint space width distribution in healthy and symptomatic subjects.
Characterization of a new animal model for evaluation and treatment of back pain due to lumbar facet joint osteoarthritis.
Vascular disease is associated with facet joint osteoarthritis.
Asporin, a susceptibility gene in osteoarthritis, is expressed at higher levels in the more degenerate human intervertebral disc.
Effect of glucosamine on pain-related disability in patients with chronic low back pain and degenerative lumbar osteoarthritis: a randomized controlled trial.
Kinetic magnetic resonance imaging analysis of abnormal segmental motion of the functional spine unit.
The contribution of spinal glial cells to chronic pain behaviour in the monosodium iodoacetate model of osteoarthritic pain.
Lumbar spine: reliability of MR imaging findings.
Infarction, Posterior Cerebral Artery
Hemoglobin SC Disease
Chromosome translocations: dangerous liaisons revisited.
Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia.
Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial.
The molecular genetics of Philadelphia chromosome-positive leukemias.
Diagnosis of chronic myeloid and acute lymphocytic leukemias by detection of leukemia-specific mRNA sequences amplified in vitro.
The biology of chronic myeloid leukemia.
In vitro transformation of immature hematopoietic cells by the P210 BCR/ABL oncogene product of the Philadelphia chromosome.
Genetic and epigenetic silencing of microRNA-203 enhances ABL1 and BCR-ABL1 oncogene expression.
Improved early event-free survival with imatinib in Philadelphia chromosome-positive acute lymphoblastic leukemia: a children's oncology group study.
Alternative splicing of RNAs transcribed from the human abl gene and from the bcr-abl fused gene.
Acute leukaemia in bcr/abl transgenic mice.
Evolution of human BCR-ABL1 lymphoblastic leukaemia-initiating cells.
The chronic myelogenous leukemia-specific P210 protein is the product of the bcr/abl hybrid gene.
Evolving concepts in the management of chronic myeloid leukemia: recommendations from an expert panel on behalf of the European LeukemiaNet.
Translation of the Philadelphia chromosome into therapy for CML.
Subclavian Steal Syndrome
The molecular biology of chronic myeloid leukemia.
Arthralgia, Insect Bite, Personality Change, Steatorrhea
Loose Anagen Hair Syndrome
Basal Cell Nevus Syndrome
Iron Metabolism Disorders
Paralysis, Hyperkalemic Periodic
Human endogenous retrovirus (HERV)-K transcripts in gonadoblastomas and gonadoblastoma-derived germ cell tumours.
Gonadoblastoma in a patient with del(9)(p22) and sex reversal: report of a case and review of the literature.
Expression pattern of a gonadoblastoma candidate gene suggests a role of the Y chromosome in prostate cancer.
Stem cell factor as a novel diagnostic marker for early malignant germ cells.
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma.
OCT4: a novel biomarker for dysgerminoma of the ovary.
DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutations.
TSPY, the candidate gonadoblastoma gene on the human Y chromosome, has a widely expressed homologue on the X - implications for Y chromosome evolution.
Molecular mapping of the putative gonadoblastoma locus on the Y chromosome.
A Cre gene directed by a human TSPY promoter is specific for germ cells and neurons.
Human testicular (non)seminomatous germ cell tumours: the clinical implications of recent pathobiological insights.
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD).
Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome.
Gonadoblastoma, testicular and prostate cancers, and the TSPY gene.
Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
Expression and interdependencies of pluripotency factors LIN28, OCT3/4, NANOG and SOX2 in human testicular germ cells and tumours of the testis.
Global gene expression responses to waterlogging in roots and leaves of cotton (Gossypium hirsutum L.).
A possible role for taurine in osmoregulation within the brain.
Exercise-associated hyponatremia: a review.
Oral water intoxication in infants. An American epidemic.
Thyroid transcription factor-1 facilitates cerebrospinal fluid formation by regulating aquaporin-1 synthesis in the brain.
Fluid overload at initiation of renal replacement therapy is associated with lack of renal recovery in patients with acute kidney injury.
Fluid overload and acute renal failure in pediatric stem cell transplant patients.
Polydipsia and water intoxication in psychiatric patients: a review of the epidemiological literature.
Water intoxication: a possible complication during endurance exercise.
Water intoxication; differential diagnosis of the hypotonic syndromes.
Transcription factor tonicity-responsive enhancer-binding protein (TonEBP) which transactivates osmoprotective genes is expressed and upregulated following acute systemic hypertonicity in neurons in brain.
BACTERIAL MENINGITIS--A REVIEW OF SELECTED ASPECTS. II. SPECIAL NEUROLOGIC PROBLEMS, POSTMENINGITIC COMPLACATIONS AND CLINICOPATHOLOGICAL CORRELATIONS.
Glial cell aquaporin-4 overexpression in transgenic mice accelerates cytotoxic brain swelling.
Aquaporin-4 and brain edema.
Association between preference for sweets and excessive alcohol intake: a review of animal and human studies.
Opioid peptides and the control of human ingestive behaviour.
In vivo measurement of brain extracellular space diffusion by cortical surface photobleaching.
Three distinct roles of aquaporin-4 in brain function revealed by knockout mice.