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459201 to 459300 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
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.
Glycogen metabolism and glycogen-storage diseases.
Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.
Familial phosphofructokinase deficiency is associated with a disturbed calcium homeostasis in erythrocytes.
Heterogeneity of the molecular lesions in inherited phosphofructokinase deficiency.
Functional expression of human mutant phosphofructokinase in yeast: genetic defects in French Canadian and Swiss patients with phosphofructokinase deficiency.
A 5' splice junction mutation leading to exon deletion in an Ashkenazic Jewish family with phosphofructokinase deficiency (Tarui disease).
Muscle phosphofructokinase deficiency: abnormal polysaccharide in a case of late-onset myopathy.
Isozymes of phosphofructokinase.
Phosphofructokinase deficiency; past, present and future.
Genetic defect in muscle phosphofructokinase deficiency. Abnormal splicing of the muscle phosphofructokinase gene due to a point mutation at the 5'-splice site.
PRKACB and Carney complex.
Lymphatics and D2-40/podoplanin expression in gastrointestinal stromal tumours of the stomach with and without lymph node metastasis: an immunohistochemical study with special reference to the Carney triad.
Large-cell calcifying Sertoli cell tumors of the testes in pediatrics.
In vitro studies of novel PRKAR1A mutants that extend the predicted RIα protein sequence into the 3'-untranslated open reading frame: proteasomal degradation leads to RIα haploinsufficiency and Carney complex.
Genetic predisposition to peripheral nerve neoplasia: diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes.
Differential role of PKA catalytic subunits in mediating phenotypes caused by knockout of the Carney complex gene Prkar1a.
Pancreatic ductal and acinar cell neoplasms in Carney complex: a possible new association.
Carney complex and other conditions associated with micronodular adrenal hyperplasias.
Adrenocortical cancer in Carney complex: a paradigm of endocrine tumor progression or an association of genetic predisposing factors?
The epidemiology and genetics of pituitary adenomas.
Carney complex: Clinical and genetic 2010 update.
Carney complex with adrenal cortical carcinoma.
A large family with Carney complex caused by the S147G PRKAR1A mutation shows a unique spectrum of disease including adrenocortical cancer.
Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer.
Clinical and molecular genetics of Carney complex.
Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update.
SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors.
Gastric stromal tumors in Carney triad are different clinically, pathologically, and behaviorally from sporadic gastric gastrointestinal stromal tumors: findings in 104 cases.
Palpitations, hypotension, hypokalemia, and hyperlactatemia. Putting the pieces together.
Metformin accumulation without hyperlactataemia and metformin-induced hyperlactataemia without metformin accumulation.
Hyperlactemia induction modes affect the lactate minimum power and physiological responses in cycling.
Lactate in sepsis.
Hyperlactatemia is an independent predictor of mortality and denotes distinct subtypes of severe sepsis and septic shock.
Glycogen storage disease type III in Egyptian children: a single centre clinico-laboratory study.
False hyperlactatemia in life-threatening ethylene glycol poisoning.
Blood lactate in HIV-infected children on antiretroviral therapy in rural South Africa.
Autism and intellectual disability associated with mitochondrial disease and hyperlactacidemia.
Association between hyperlactatemia and occult cardiac failure in diabetic patients on maintenance hemodialysis.
Advances in acute asthma.
[Relation between metformin treatment and the development of hyperlactacidemia at the emergency room].
The relationship between hyperlactatemia and microcirculation in the thenar eminence as measured using near-infrared spectroscopy in patients with sepsis.
Lactate, blood pressure and infection: tied by faith, untied by man?
Investigating sepsis with biomarkers.
Even mild hyperlactatemia is associated with increased mortality in critically ill patients.
Effects of diet-induced obesity and voluntary exercise in a tauopathy mouse model: implications of persistent hyperleptinemia and enhanced astrocytic leptin receptor expression.
Abnormal resting blood lactate. I. The significance of hyperlactatemia in hospitalized patients.
Localization of post-traumatic trochlear nerve palsy associated with hemorrhage at the subarachnoid space by magnetic resonance imaging.
Magnetic resonance imaging of the superior oblique muscle in superior oblique myokymia.
Limitations of brain stem auditory evoked potentials for intraoperative monitoring during a posterior fossa operation: case report and technical note.
Hypertropia following trochlear trauma.
Fourth nerve palsy: historical review and study of 215 inpatients.
Fourth cranial nerve palsy in a collegiate lacrosse player: a case report.
Diplopia following head injury.
[Decompensated strabismus surso-adductorius].
Traumatic trochlear nerve palsy following minor occipital impact--four case reports.
Aetiology and outcomes of adult superior oblique palsies: a modern series.
Central trochlear palsy.
Acquired lesions of the fourth cranial nerve.
Degenerative and regenerative changes in the trochlear nerve of goldfish.
[Preservation of olfaction in bifrontal craniotomies for lesions of the anterior and middle cranial fossa].
[CSF leakage and anosmia in aneurysm clipping of anterior communicating artery by basal interhemispheric approach].
Thallium transport and the evaluation of olfactory nerve connectivity between the nasal cavity and olfactory bulb.
Postoperative anosmia after anterior communicating artery aneurysms surgery by the pterional approach.
Peak in matrix metaloproteinases-2 levels observed during recovery from olfactory nerve injury.
Neuronal nitric oxide synthase in the olfactory system of an adult teleost fish Oreochromis mossambicus.
Microsurgical anatomic features of the olfactory nerve: relevance to olfaction preservation in the pterional approach.
Administration of transforming growth factor-alpha enhances anatomical and behavioral recovery following olfactory nerve transection.
Posttraumatic olfactory dysfunction: MR and clinical evaluation.
Post-traumatic anosmia. Ultrastructural correlates.
Hyposmia following laryngectomy.
Rhinotopy is disrupted during the re-innervation of the olfactory bulb that follows transection of the olfactory nerve.
Altered expression and localization of ion transporters contribute to diarrhea in mice with Salmonella-induced enteritis.
Post-traumatic olfactory dysfunction.
Olfactory nerve recovery following mild and severe injury and the efficacy of dexamethasone treatment.
Temporal profiling of gene expression during neurogenesis and remodeling in the olfactory epithelium at short intervals after target ablation.
An updated review of clinical olfaction.
Sensory experience selectively regulates transmitter synthesis enzymes in interglomerular circuits.
BIG-2 mediates olfactory axon convergence to target glomeruli.
Ophthalmic complications associated with orthognathic surgery.