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507101 to 507200 most common queries
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Inflammatory monocytes facilitate adaptive CD4 T cell responses during respiratory fungal infection.
Broncho-pulmonary aspergillosis; a review and a report of eight new cases.
Calcifying epithelial odontogenic tumour: biological profile based on 181 cases from the literature.
Expression of odontogenic ameloblast-associated protein (ODAM) in dental and other epithelial neoplasms.
Relative incidence of odontogenic tumors and oral and jaw cysts in a Canadian population.
Transgenic mice that express normal and mutated amelogenins.
Characterization of Apin, a secreted protein highly expressed in tooth-associated epithelia.
Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.
C Edith Juárez-Maldonado
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.
Nuclear localization of the parafibromin tumor suppressor protein implicated in the hyperparathyroidism-jaw tumor syndrome enhances its proapoptotic function.
Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias.
Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31.
Metastatic tumours to the oral cavity - pathogenesis and analysis of 673 cases.
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome.
Immunoglobulin and glucose-6-phosphate dehydrogenase as markers of cellular origin in Burkitt lymphoma.
Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds.
DNA of Epstein-Barr virus detected in tissue of Burkitt's lymphoma and nasopharyngeal carcinoma.
Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome.
A sarcoma involving the jaws in African children.
Adamantinoma (so-called) of the long bones; review of the literature and report of three new cases.
Dentigerous cysts of inflammatory origin. A clinicopathologic study.
Bilateral maxillary dentigerous cysts: a case report.
Dentigerous cyst associated with multiple mesiodens: a case report.
Bilateral dentigerous cysts--report of an unusual case and review of the literature.
Anterior maxillary supernumerary teeth: a clinical and radiographic study.
STUDIES ON ODONTOGENIC CYST EPITHELIUM. 2. CLINICAL AND ROENTGENOLOGIC ASPECTS OF ODONTOGENIC KERATOCYSTS.
Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.
Central odontogenic fibroma of mandible: a case report and review of the literature.
Adenomatoid odontogenic tumor arising in a dental cyst: report of unusual case.
The odontogenic keratocyst: orthokeratinized variant.
Periodontal tissue disposition of azithromycin in patients affected by chronic inflammatory periodontal diseases.
Marsupialization as a definitive treatment for the odontogenic keratocyst.
A calcifying epithelial odontogenic tumor.
The odontogenic keratocyst. A clinicopathologic study of 312 cases. Part II. Histologic features.
Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome.
Cloning and characterization of the human ameloblastin gene.
Ameloblastomas of the jaws.
Adipose stem cell tissue-engineered construct used to treat large anterior mandibular defect: a case report and review of the clinical application of good manufacturing practice-level adipose stem cells for bone regeneration.
Oral and maxillofacial tumours in children: a review.
Odontogenic tumors: a study of 1309 cases in a Chinese population.
Malignant ameloblastoma or ameloblastic carcinoma.
Gene expression profiling of ameloblastoma and human tooth germ by means of a cDNA microarray.
Melanotic neuroectodermal tumor of infancy--a neoplasm of neural crese origin. Report of a case associated with high urinary excretion of vanilmandelic acid.
Carcnogenicity of epoxides, lactones, and peroxy compounds. VI. Structure and carcinogenic activity.
Unicystic ameloblastoma. A review of 193 cases from the literature.
Tae Jung Jang
Odontogenic tumors in Mexico: a collaborative retrospective study of 349 cases.
Ameloblastoma: biological profile of 3677 cases.
The results of transplantation of intercalary allografts after resection of tumors. A long-term follow-up study.
Relative frequency of central odontogenic tumors: a study of 1,088 cases from Northern California and comparison to studies from other parts of the world.
Autoimmune hair loss (alopecia areata) transferred by T lymphocytes to human scalp explants on SCID mice.
Critical role of heparin binding domains of ameloblastin for dental epithelium cell adhesion and ameloblastoma proliferation.
Alopecia areata induced in C3H/HeJ mice by interferon-gamma: evidence for loss of immune privilege.
On the etiology of vitiligo and gray hair.
Guidelines for the management of alopecia areata.
Maintenance of hair follicle immune privilege is linked to prevention of NK cell attack.
Adult-onset Alopecia areata is a complex polygenic trait in the C3H/HeJ mouse model.
Alopecia areata update.
Experimental induction of alopecia areata-like hair loss in C3H/HeJ mice using full-thickness skin grafts.
Vitiligo, thyroid disease and autoimmunity.
Treatment of hair loss.
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.
Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21.
Lymphocytes, neuropeptides, and genes involved in alopecia areata.
ALOPECIA AREATA. AN EVALUATION OF 736 PATIENTS.
Alopecia areata in aging C3H/HeJ mice.
Incidence of alopecia areata in Olmsted County, Minnesota, 1975 through 1989.
A short form of the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12).
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.
The prevalence of pelvic floor disorders and their relationship to gender, age, parity and mode of delivery.
Signs of genital prolapse in a Swedish population of women 20 to 59 years of age and possible related factors.
The demographics of pelvic floor disorders: current observations and future projections.
Anatomic aspects of vaginal eversion after hysterectomy.
Pelvic Organ Support Study (POSST): the distribution, clinical definition, and epidemiologic condition of pelvic organ support defects.
Abdominal sacrocolpopexy: a comprehensive review.
Epidemiology of genital prolapse: observations from the Oxford Family Planning Association Study.
Comparison of levator ani muscle defects and function in women with and without pelvic organ prolapse.
Melanosis of the esophagus.
Malignant melanoma in England: risks associated with naevi, freckles, social class, hair colour, and sunburn.
squeezing, pressure, tension headache, with, burning, crawling sensations, on scalp, neck stiffness, mental, delirium, facial pain, chronic headache, bilateral, severe headache with sudden onset, recurrent headache, acute, chronic pain
Cutaneous factors related to the risk of malignant melanoma.
Pigmentation and skin reaction to sun as risk factors for cutaneous melanoma: Western Canada Melanoma Study.
Melanism in peromyscus is caused by independent mutations in agouti.
Albinism and skin cancer in Southern Africa.
From PGF(2alpha)-isopropyl ester to latanoprost: a review of the development of xalatan: the Proctor Lecture.
The melanocortin-1-receptor gene is the major freckle gene.
Surgical management of conjunctival tumors. The 1994 Lynn B. McMahan Lecture.
Suntan, sunburn, and pigmentation factors and the frequency of acquired melanocytic nevi in children. Similarities to melanoma: the Vancouver Mole Study.
Chronic arsenic toxicity in Bangladesh and West Bengal, India--a review and commentary.
Risk of cutaneous melanoma associated with pigmentation characteristics and freckling: systematic overview of 10 case-control studies. The International Melanoma Analysis Group (IMAGE).
Exposure to sunlight and other risk factors for age-related macular degeneration.
Personal risk-factor chart for cutaneous melanoma.
Different genes underlie adaptive melanism in different populations of rock pocket mice.
Murine cutaneous mastocytosis and epidermal melanocytosis induced by keratinocyte expression of transgenic stem cell factor.
The genetic basis of adaptive melanism in pocket mice.
Retinal Necrosis Syndrome, Acute