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460801 to 460900 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Black piedra in a child with pili torti, bamboo hair and congenital ichthyosiform erythroderma.
White piedra--a case report and review of the literature.
White piedra in children.
Genital white piedra: epidemiology, microbiology, and therapy.
A study of 3891 cases of mycoses in the tropics.
White piedra and Trichosporon species in equatorial Africa. II. Clinical and mycological associations: an analysis of 449 superficial inguinal specimens.
White piedra and Trichosporon species in equatorial Africa. I. History and clinical aspects: an analysis of 449 superficial inguinal specimens.
Structural abnormalities of the hair shaft.
A new Brevibacterium sp. isolated from infected genital hair of patients with white piedra.
Superficial mycoses in immunodepressed patients (AIDS).
Superficial fungal infections.
The power of the extreme in elucidating obesity.
Taxonomic position of deep-seated, mucosa-associated, and superficial isolates of Trichosporon cutaneum from trichosporonosis patients.
Obesity: a new feature of WAGR (del 11p) syndrome.
Genetic and hereditary aspects of childhood obesity.
Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic map.
Characterization of an evolutionarily conserved metallophosphoesterase that is expressed in the fetal brain and associated with the WAGR syndrome.
Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes.
Altered trans-activational properties of a mutated WT1 gene product in a WAGR-associated Wilms' tumor.
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
Recent advances in Wilms tumor genetics.
Congenital diaphragmatic hernia in WAGR syndrome.
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis.
Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study Group.
Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
Missense mutations in the DNA-binding region and termination codon in PAX6.
WAGR syndrome: a clinical review of 54 cases.
Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders.
Aniridia: current pathology and management.
A clinical overview of WT1 gene mutations.
Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
Functional outcome after surgical treatment of spontaneous and nonspontaneous spinal subdural hematomas.
Difficulties diagnosing spinal subdural hemorrhage in a hypo-coagulated patient due to simultaneous symptomatic subdural cranial hemorrhage.
Con: Surgery should not proceed when a bloody tap occurs during spinal drain placement for elective thoracoabdominal aortic surgery.
Complications following large-volume epidural blood patches for postdural puncture headache. Lumbar subdural hematoma and arachnoiditis: initial cause or final effect?
Chronic cervicothoracic spinal subdural hematoma.
As sharp as Occam?
A case report of rapid spontaneous redistribution of acute supratentorial subdural hematoma to the entire spinal subdural space presenting as a Pourfour du Petit syndrome and review of the literature.
[Spinal subdural haematoma].
[Incidence in Catalonia of spinal cord compression due to spinal hematoma secondary to neuraxial anesthesia].
Use of topically applied rt-PA in the evacuation of extensive acute spinal subdural haematoma.
Traumatic subdural hematoma of the thoraco-lumbar junction of spinal cord.
Spontaneous concomitant cranial and spinal subdural haematomas with spontaneous resolution.
Spinal chronic subdural hematoma in association with anticoagulant therapy: a case report and literature review.
Neurological complications following central neuraxial blockades in obstetrics.
Lumbosacral subdural hematoma. Case report.
Dissecting aneurysm of the thoracic posterior spinal artery. Case illustration.
Rapid spontaneous remission of a spontaneous spinal chronic subdural hematoma in a child.
MRI findings in spinal subdural and epidural hematomas.
Acute spontaneous spinal subdural hematoma presenting as paraplegia: a rare case.
Posterior triangle operations and trapezius paralysis.
Late sequelae of iatrogenic spinal accessory nerve injury.
Conduction studies along the accessory nerve and follow-up of patients with trapezius palsy.
Biting palsy of the accessory nerve.
Accessory nerve palsy.
The spinal accessory nerve plexus, the trapezius muscle, and shoulder stabilization after radical neck cancer surgery.
Spinal accessory nerve injury.
Reduction of shoulder disability after neck dissection.
Anasarca, Cachexia, Marasmus
Extracranial spinal accessory nerve injury.
Nerve injuries about the shoulder in sports.
Acessory nerve function after surgical procedures in the posterior triangle.
Accessory spinal nerve injury.
Peripheral nerve injuries in athletes. Treatment and prevention.
Nerve injury about the shoulder in athletes, part 2: long thoracic nerve, spinal accessory nerve, burners/stingers, thoracic outlet syndrome.
Functional evaluation of the spinal accessory nerve after neck dissection.
Uncoupling protein-1 mRNA expression in lipomas from patients bearing pathogenic mitochondrial DNA mutations.
Restoration of normal BMP signaling levels and osteogenic differentiation in FOP mesenchymal progenitor cells by mutant allele-specific targeting.
Neuropathy in multiple symmetric lipomatosis. Madelung's disease.
Multiple symmetric lipomatosis (Launois-Bensaude syndrome): effect of oral salbutamol.
Multiple lipomas, alcoholism, and neuropathy: Madelung's disease or MERRF?
Madelung-like deformity in pseudohypoparathyroidism type 1b.
Madelung disease: a not-so-rare disorder.
Genotypes and phenotypes of children with SHOX deficiency in France.
FATTY INFILTRATION OF THE MEDIAN NERVE.
Differential clinical expression of multiple symmetric lipomatosis in men and women.
Scoliosis, Subnormal Intelligence
Adiponectin, resistin and subclinical inflammation--the metabolic burden in Launois Bensaude Syndrome, a rare form of obesity.
Ultrasound assisted liposuction for the palliative treatment of Madelung's disease: a case report.
Multiple symmetric lipomatosis. Ultrastructural investigation of the tissue and preadipocytes in primary culture.
Multiple symmetric lipomatosis may be the consequence of defective noradrenergic modulation of proliferation and differentiation of brown fat cells.
Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports.
Lipolysis of lipomas in patients with familial multiple lipomatosis: an ultrasonography-controlled trial.
Fat distribution in AIDS.
Benign symmetric lipomatosis (Madelung's disease): case reports and current management.
Multiple symmetric lipomatosis: clinical aspects and outcome in a long-term longitudinal study.
Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophy.
Vocal Cord Dysfunction
Mutations in muscle phosphofructokinase gene.
Muscle phosphofructokinase deficiency in two generations.
Fatal infantile form of muscle phosphofructokinase deficiency.
Characterization of the enzymatic defect in late-onset muscle phosphofructokinase deficiency. New subtype of glycogen storage disease type VII.
Tissue-dependent loss of phosphofructokinase-M in mice with interrupted activity of the distal promoter: impairment in insulin secretion.
Muscle glycogenoses: an overview.
Isozymes of human phosphofructokinase: biochemical and genetic aspects.
Phosphofructo-1-kinase deficiency leads to a severe cardiac and hematological disorder in addition to skeletal muscle glycogenosis.
Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency.