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496001 to 496100 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Renal tubular malfunction and pulmonary emphysema in cadmium pigment workers.
JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia.
Polycythemia vera: stem-cell and probable clonal origin of the disease.
TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis.
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms.
Efficacy of TG101348, a selective JAK2 inhibitor, in treatment of a murine model of JAK2V617F-induced polycythemia vera.
Safety and efficacy of TG101348, a selective JAK2 inhibitor, in myelofibrosis.
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel.
JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis.
Ratio of mutant JAK2-V617F to wild-type Jak2 determines the MPD phenotypes in transgenic mice.
Expression of Jak2V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model.
Graft-versus-leukemia effect of donor lymphocyte transfusions in marrow grafted patients.
Identification of an acquired JAK2 mutation in polycythemia vera.
Abdominal Pain, Hepatosplenomegaly, Vesicular Rash, blood in stool, chronic pain, acute rash, fever, focal
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.
Congenital intestinal atresia and severe stenosis in the newborn; a report on 79 consecutive cases.
Use of benzodiazepines and benzodiazepine receptor agonists during pregnancy: neonatal outcome and congenital malformations.
Familial jejunal atresia: three cases in one family.
Copper deficiency in long-term parenteral nutrition.
Colonic atresia without mesenteric vascular occlusion. The role of the fibroblast growth factor 10 signaling pathway.
Vancomycin-resistant Pediococcus acidilactici: nine cases of bacteremia.
Maternal medication use and risks of gastroschisis and small intestinal atresia.
First-trimester drug use and congenital disorders.
Study of Down syndrome in 238,942 consecutive births.
Neonatal short bowel syndrome: a cohort study.
Factors correlating with a successful outcome following extensive intestinal resection in newborn infants.
Growth and development of an infant receiving all nutrients exclusively by vein.
Congenital intestinal atresia and stenosis in the newborn. Observations on its pathogenesis and treatment.
Abdominal Pain, Hepatosplenomegaly, Vesicular Rash, blood in stool, chronic pain, acute rash, fever
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
Asbestos exposure, pleural mesothelioma, and serum osteopontin levels.
Chrysotile asbestos inhalation in rats: deposition pattern and reaction of alveolar epithelium and pulmonary macrophages.
A role for the receptor for advanced glycation end products in idiopathic pulmonary fibrosis.
Enhanced IL-1 beta and tumor necrosis factor-alpha release and messenger RNA expression in macrophages from idiopathic pulmonary fibrosis or after asbestos exposure.
The role of free radicals in asbestos-induced diseases.
Expression of cyclooxygenase-2 in human lung carcinoma.
Mechanisms in the pathogenesis of asbestosis and silicosis.
Carbon nanotubes introduced into the abdominal cavity of mice show asbestos-like pathogenicity in a pilot study.
Phytophotodermatitis: a sometimes difficult diagnosis.
Photosensitivity to exogenous agents.
Photosensitivity and antinuclear antibodies in black patients with systemic lupus erythematosus.
Photoallergic contact dermatitis from topical diclofenac in Solaraze gel.
Liver transplantation for erythropoietic protoporphyria. Report of a new case with subsequent medium-term follow-up.
Hereditary photosensitivity of the American Indian.
Evaluation of phototoxic and photoallergic potentials of 13 compounds by different in vitro and in vivo methods.
Duration of skin photosensitivity and incidence of photosensitivity reactions after administration of verteporfin.
Drug-induced photosensitivity: culprit drugs, management and prevention.
Phototoxicity and photoallergy.
Interferon-gamma is involved in photoimmunoprotection by UVA (320-400 nm) radiation in mice.
Human dermal safety studies with eflornithine HCl 13.9% cream (Vaniqa), a novel treatment for excessive facial hair.
Contact and photocontact sensitivity to sunscreens. Review of a 15-year experience and of the literature.
The first case of efavirenz-induced photosensitivity in a Japanese patient with HIV infection.
Hydroa vacciniforme: A clinical and follow-up study of 17 cases.
Photocontact dermatitis and chloracne: two major occupational and environmental skin diseases induced by different actions of halogenated chemicals.
Cutaneous photosensitivity diseases induced by exogenous agents.
Drug photosensitivity, idiopathic photodermatoses, and sunscreens.
Kimura disease involving parotid gland and cervical nodes: CT and MR findings.
Association of galectin-9 with eosinophil apoptosis.
Abdominal Pain, Hepatosplenomegaly, Vesicular Rash, blood in stool, chronic pain, acute rash
Angiolymphoid hyperplasia with eosinophilia associated with tetanus toxoid vaccination.
T and B lymphocytes with immunoglobulin E Fc receptors (Fc epsilon R) in patients with nonallergic hyperimmunoglobulinemia E: demonstration using a monoclonal antibody against Fc epsilon R-associated antigen.
J M Balog
Observations concerning the pathogenesis of epithelioid hemangioma (angiolymphoid hyperplasia).
Radiation therapy in Kimura's disease.
Nephrotic syndrome associated with Kimura disease.
Kimura's disease: two case reports and a literature review.
Kimura's disease and angiolymphoid hyperplasia with eosinophilia: clinical and histopathologic differences.
Angiolymphoid hyperplasia with eosinophilia (Kimura's disease) of the orbit.
In vivo expression of IL-4, IL-5, IL-13 and IFN-gamma mRNAs in peripheral blood mononuclear cells and effect of cyclosporin A in a patient with Kimura's disease.
Epithelioid hemangioma versus Kimura's disease. A comparative clinicopathologic study.
Kimura's disease and angiolymphoid hyperplasia with eosinophilia: two distinct histopathological entities.
Kimura's disease. Involvement of regional lymph nodes and distinction from angiolymphoid hyperplasia with eosinophilia.
Lymphadenopathy of Kimura's disease.
Kimura disease: a clinicopathologic study of 21 cases.
Angiolymphoid hyperplasia with eosinophilia. A clinicopathologic study of 116 patients.
Hypokalemic Periodic Paralysis
Abdominal Pain, Hepatosplenomegaly, Vesicular Rash, blood in stool, chronic pain
Measles as an index of immunological function.
Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Globoid cell leucodystrophy (Krabbe's disease): deficiency of galactocerebroside beta-galactosidase.
Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
Progressive multifocal leukoencephalopathy.
Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.
POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion.
Alpha B-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain.
Isolation of measles virus from cell cultures of brain from a patient with subacute sclerosing panencephalitis.
Subacute sclerosing panencephalitis: isolation of measles virus from a brain biopsy.
Measles-virus antibody and antigen in subacute sclerosing panencephalitis.
Embryonic stem cell-derived glial precursors: a source of myelinating transplants.
K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation.
Ion-channel defects and aberrant excitability in myotonia and periodic paralysis.
Acquired neuromyotonia: evidence for autoantibodies directed against K+ channels of peripheral nerves.
Myotonia fluctuans. A third type of muscle sodium channel disease.
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH.