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Guanylin and functional coupling proteins in the human salivary glands and gland tumors : expression, cellular localization, and target membrane domains.
Osteomyelitis of the mandible associated with autosomal dominant osteopetrosis: a case report.
Cytogenetic analysis of salivary gland type tumors.
Implications of tooth root hypercementosis in a Barbados slave skeletal collection.
Identification of oncocytic lesions of salivary glands by anti-mitochondrial immunohistochemistry.
Effect of HIP/ribosomal protein L29 deficiency on mineral properties of murine bones and teeth.
Clinical analysis of salivary gland tumor cases in West China in past 50 years.
Alveolar bone loss of senescence-accelerated mouse (SAM).
Salivary gland tumors in a Brazilian population: a retrospective study of 124 cases.
A scanning electron microscopic study of hypercementosis.
Studies of dental root surface caries. 2: The role of cementum in root surface caries.
Cemento-osseous dysplasia of the jaws in 54 Japanese patients: a radiographic study.
Parotid gland tumors: can addition of diffusion-weighted MR imaging to dynamic contrast-enhanced MR imaging improve diagnostic accuracy in characterization?
Histogenic classification of salivary tumors.
Differentiation of benign and malignant parotid tumors using deconvolution-based perfusion CT imaging: feasibility of the method and initial results.
Immunolocalization of matrix metalloproteinases-2 and -9 during apical periodontitis development.
Histogenesis of papillary cystadenoma lymphomatosum (Warthin's tumor) of the parotid salivary gland.
Benign and malignant oncocytoma.
A study of MECT1-MAML2 in mucoepidermoid carcinoma and Warthin's tumor of salivary glands.
Fine-needle aspiration cytology of salivary gland: a review of 341 cases.
Recoverin-associated retinopathy: a clinically and immunologically distinctive disease.
Detection of damage to the mitochondrial genome in the oncocytic cells of Warthin's tumour.
CRTC1/MAML2 fusion transcript in high grade mucoepidermoid carcinomas of salivary and thyroid glands and Warthin's tumors: implications for histogenesis and biologic behavior.
Altered Notch signaling resulting from expression of a WAMTP1-MAML2 gene fusion in mucoepidermoid carcinomas and benign Warthin's tumors.
A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type I.
Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletion.
New perspectives on the molecular basis of hereditary bone tumours.
Constipation, Episodic Scotomas, Low Self-Esteem
Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome.
Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III.
Clinical and molecular characterization of a patient with Langer-Giedion syndrome and mosaic del(8)(q22.3q24.13).
A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).
Missense mutation of TRPS1 in a family of tricho-rhino-phalangeal syndrome type III.
Further case of microdeletion of 8q24 with phenotype overlapping Langer-Giedion without TRPS1 deletion.
Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes.
Classification of osteogenesis imperfecta by dental characteristics.
Construction and characterization of band-specific DNA libraries.
Genetic evidence for key roles of decorin and biglycan in dentin mineralization.
Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.
Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome.
Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II.
Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.
Chest Pain, Rectal Bleeding, Volvulus, chest pain worse on breathing, diarrhea, dyschezia, blood in stool, acute diarrhea, abdominal pain, flatulence, pyrosis, chest pain rectal bleeding constipation and dirreah headaches depression
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.
Hereditary multiple exostoses.
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I.
The carboxyl-terminal domain of phosphophoryn contains unique extended triplet amino acid repeat sequences forming ordered carboxyl-phosphate interaction ridges that may be essential in the biomineralization process.
The importance of intrafibrillar mineralization of collagen on the mechanical properties of dentin.
The gene associated with trichorhinophalangeal syndrome in humans is overexpressed in breast cancer.
A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.
DSPP mutation in dentinogenesis imperfecta Shields type II.
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III.
Metastatic and histologic presentations in unknown primary cancer.
Low values of 5-hydroxymethylcytosine (5hmC), the "sixth base," are associated with anaplasia in human brain tumors.
Loss of p53 promotes anaplasia and local invasion in ret/PTC1-induced thyroid carcinomas.
Gangliogliomas: an intriguing tumor entity associated with focal epilepsies.
Structural and functional changes of normal aging skin.
Smooth muscle tumors of the gastrointestinal tract. What we know now that Stout didn't know.
Anaplastic large cell Ki-1 lymphoma. Delineation of two morphological types.
The TP53-ARF tumor suppressor pathway is frequently disrupted in large/cell anaplastic medulloblastoma.
Gliomas: classification with MR imaging.
Comparative genomic hybridization detects an increased number of chromosomal alterations in large cell/anaplastic medulloblastomas.
Skin diseases in south-east Nigeria: a current perspective.
c-myc overexpression causes anaplasia in medulloblastoma.
Depression and suicidal behavior in acne patients treated with isotretinoin: a systematic review.
Histopathological and molecular prognostic markers in medulloblastoma: c-myc, N-myc, TrkC, and anaplasia.
Acquired trichomegaly and symptomatic external ocular changes in patients receiving epidermal growth factor receptor inhibitors: case reports and a review of literature.
Histopathologic grading of medulloblastomas: a Pediatric Oncology Group study.
Histopathology and prognosis of Wilms tumors: results from the First National Wilms' Tumor Study.
Effect of treatment with a colloidal oatmeal lotion on the acneform eruption induced by epidermal growth factor receptor and multiple tyrosine-kinase inhibitors.
Anti-EGFR mechanism of action: antitumor effect and underlying cause of adverse events.
Id family of helix-loop-helix proteins in cancer.
Microarray analysis of gene expression in peripheral blood mononuclear cells from dioxin-exposed human subjects.
Common side effects of anti-EGFR therapy: acneform rash.
Interdisciplinary management of EGFR-inhibitor-induced skin reactions: a German expert opinion.
Consensus guidelines for the management of radiation dermatitis and coexisting acne-like rash in patients receiving radiotherapy plus EGFR inhibitors for the treatment of squamous cell carcinoma of the head and neck.
Acneiform eruption induced by epidermal growth factor receptor inhibitors in patients with solid tumours.
Severe 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) intoxication: clinical and laboratory effects.
Uncovering Pandora's vase: the growing problem of new toxicities from novel anticancer agents. The case of sorafenib and sunitinib.
Phase II trial of single agent cetuximab in patients with persistent or recurrent epithelial ovarian or primary peritoneal carcinoma with the potential for dose escalation to rash.
Dioxin-induced chloracne--reconstructing the cellular and molecular mechanisms of a classic environmental disease.
Randomized double-blind trial of prophylactic oral minocycline and topical tazarotene for cetuximab-associated acne-like eruption.
Suboccipital injection with a mixture of rapid- and long-acting steroids in cluster headache: a double-blind placebo-controlled study.
Treatment of philadelphia chromosome-positive, accelerated-phase chronic myelogenous leukemia with imatinib mesylate.
Occipital nerve stimulation for drug-resistant chronic cluster headache: a prospective pilot study.
The role of nitric oxide (NO) in migraine, tension-type headache and cluster headache.
Cluster headache: pathogenesis, diagnosis, and management.
Cluster headache prevalence. Vågå study of headache epidemiology.
The trigeminovascular system in humans: pathophysiologic implications for primary headache syndromes of the neural influences on the cerebral circulation.
Survival benefit with imatinib mesylate therapy in patients with accelerated-phase chronic myelogenous leukemia--comparison with historic experience.
Increase in plasma calcitonin gene-related peptide from the extracerebral circulation during nitroglycerin-induced cluster headache attack.