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464501 to 464600 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Manganese and Parkinson's disease: a critical review and new findings.
Manganese action in brain function.
Manganism and idiopathic parkinsonism: similarities and differences.
Manganese toxicity upon overexposure.
Manganese neurotoxicity: a review of clinical features, imaging and pathology.
Manganese-induced parkinsonism and Parkinson's disease.
Desmoplastic small round cell tumor of the lung.
Desmoplastic small round cell tumor (DSRCT) arising in the ovary: report of a case diagnosed at an early stage and review of the literature.
Clinical outcomes of patients with desmoplastic small round cell tumor of the peritoneum undergoing autologous HCT: a CIBMTR retrospective analysis.
Analysis of prognostic factors of pediatric-type sarcomas in adult patients.
Activity of trabectidin in desmoplastic small round cell tumor.
Analysis of clinicopathological features and prognostic factors of desmoplastic small round cell tumor.
Morphoproteomic profiling of the mammalian target of rapamycin (mTOR) signaling pathway in desmoplastic small round cell tumor (EWS/WT1), Ewing's sarcoma (EWS/FLI1) and Wilms' tumor(WT1).
Metastatic desmoplastic small round cell tumor controlled by an anthracycline-based regimen: review of the role of chemotherapy.
Desmoplastic small round cell tumors with EWS-WT1 fusion transcript in children and young adults.
Desmoplastic small round cell tumor of major salivary glands: report of 1 case and a review of the literature.
Complete cytoreduction and HIPEC improves survival in desmoplastic small round cell tumor.
CT, MRI, and FDG-PET/CT imaging findings of abdominopelvic desmoplastic small round cell tumors: correlation with histopathologic findings.
[90Y]yttrium microspheres radioembolotherapy in desmoplastic small round cell tumor hepatic metastases.
Characteristic imaging features of desmoplastic small round cell tumour.
Brisk Reflexes, Drooling, Myotonic Dystrophy
Pulmonary thrombotic tumoral microangiopathy: when a presumptive diagnosis can save a life.
The diagnosis and management of desmoplastic small round cell tumor: a review.
Phase II study of ganitumab, a fully human anti-type-1 insulin-like growth factor receptor antibody, in patients with metastatic Ewing family tumors or desmoplastic small round cell tumors.
Insulin growth factor-receptor (IGF-1R) antibody cixutumumab combined with the mTOR inhibitor temsirolimus in patients with refractory Ewing's sarcoma family tumors.
Unusual oral manifestations and evolution in glycogen storage disease type Ib.
Case records of the Massachusetts General Hospital. Case 23-2007. A 9-year-old boy with bone pain, rash, and gingival hypertrophy.
The efficacy of combined treatment with prednisone and cyclosporine in patients with pemphigus: preliminary study.
Periodontal management of gingival overgrowth in the heart transplant patient: a case report.
Orofacial granulomatosis: a diagnostic problem for the unwary and a management dilemma. Case reports.
"The pill" as an etiologic agent in hypertrophic gingivitis.
Switch from cyclosporine A to mycophenolate mofetil in nephrotic children.
Medications' impact on oral health.
Heterogeneity in gingival fibromatosis.
Drug-induced gingival overgrowth.
CYP2C polymorphisms, phenytoin metabolism and gingival overgrowth in epileptic subjects.
Two cases of juvenile hyalin fibromatosis. Some histological, electron microscopic, and tissue culture observations.
Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis.
Cherubism, gingival fibromatosis, epilepsy, and mental deficiency (Ramon syndrome) with juvenile rheumatoid arthritis.
A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation.
High-dose oral cyclosporin therapy for recurrent focal segmental glomerulosclerosis in children.
Long-term seizure outcome in 211 patients with focal cortical dysplasia.
Long-duration epilepsy affects cell morphology and glutamatergic synapses in type IIB focal cortical dysplasia.
In response: Long-term seizure outcome in 211 patients with focal cortical dysplasia.
Focal cortical dysplasia type IIb in the rolandic cortex: functional reorganization after early surgery documented by passive task functional MRI.
Commentary on Long-term seizure outcome in 211 patients with focal cortical dysplasia.
Angiocentric glioma: a clinicopathologic review of 5 tumors with identification of associated cortical dysplasia.
3T MRI improves the detection of transmantle sign in type 2 focal cortical dysplasia.
Lesion focused stereotactic thermo-coagulation of focal cortical dysplasia IIB: a new approach to epilepsy surgery?
High frequency oscillations mirror disease activity in patients with focal cortical dysplasia.
Epileptogenic networks of type II focal cortical dysplasia: a stereo-EEG study.
A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II.
mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis.
Sjogren's Syndrome, vitamin b12 deficiency, mercury
The extracellular matrix and diffusion barriers in focal cortical dysplasias.
Neuroimaging in identifying focal cortical dysplasia and prognostic factors in pediatric and adolescent epilepsy surgery.
Morphometric MRI analysis improves detection of focal cortical dysplasia type II.
New variants of malignant glioneuronal tumors: a clinicopathological study of 40 cases.
Focal cortical dysplasia type IIa and IIb: MRI aspects in 118 cases proven by histopathology.
Expression and cellular distribution of multidrug transporter proteins in two major causes of medically intractable epilepsy: focal cortical dysplasia and glioneuronal tumors.
Neuropathologic measurements in focal cortical dysplasias: validation of the ILAE 2011 classification system and diagnostic implications for MRI.
Comprehensive characterization of genomic aberrations in gangliogliomas by CGH, array-based CGH and interphase FISH.
Altered inhibition in tuberous sclerosis and type IIb cortical dysplasia.
Detection of human papillomavirus in human focal cortical dysplasia type IIB.
Allopregnanolone serum levels and expression of 5 alpha-reductase and 3 alpha-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsy.
Differential cellular gene expression in ganglioglioma.
Activation of multiple molecular mechanisms for apoptosis in human malignant glioblastoma T98G and U87MG cells treated with sulforaphane.
Pi3K-mTOR signaling and AMOG expression in epilepsy-associated glioneuronal tumors.
Hyaluronate receptors mediating glioma cell migration and proliferation.
Gene therapy of intracranial glioma using interleukin 12-secreting human umbilical cord blood-derived mesenchymal stem cells.
Anemia, Carpal Tunnel Syndrome, Hypesthesia, Monoclonal Gammopathy of Undetermined Significance
Preserved function in brain invaded by tumor.
Cytogenetic analysis of 120 primary pediatric brain tumors and literature review.
Differential expression patterns of chloride transporters, Na+-K+-2Cl--cotransporter and K+-Cl--cotransporter, in epilepsy-associated malformations of cortical development.
Impaired familiarity with preserved recollection after anterior temporal-lobe resection that spares the hippocampus.
The inhalation anesthetic isoflurane induces a vicious cycle of apoptosis and amyloid beta-protein accumulation.
Disruption of TBC1D7, a subunit of the TSC1-TSC2 protein complex, in intellectual disability and megalencephaly.
Macrocephaly as a clinical indicator of genetic subtypes in autism.
Autistic spectrum disorder in a 9-year-old girl with macrocephaly.
The phenotype of recurrent 10q22q23 deletions and duplications.
Mitochondrial dysfunction in Pten haplo-insufficient mice with social deficits and repetitive behavior: interplay between Pten and p53.
Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly.
Mutant GlialCAM causes megalencephalic leukoencephalopathy with subcortical cysts, benign familial macrocephaly, and macrocephaly with retardation and autism.
Megalencephaly syndromes and activating mutations in the PI3K-AKT pathway: MPPH and MCAP.
Macrocephaly in children with autism spectrum disorders.
Generation of an ICF syndrome model by efficient genome editing of human induced pluripotent stem cells using the CRISPR system.
Principal pathogenetic components and biological endophenotypes in autism spectrum disorders.
Disruptive CHD8 mutations define a subtype of autism early in development.
Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis.
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, regurgitation
Analysis of prevalence and degree of macrocephaly in patients with germline PTEN mutations and of brain weight in Pten knock-in murine model.
DUF1220-domain copy number implicated in human brain-size pathology and evolution.
Early generalized overgrowth in boys with autism.
Sustained activation of mTOR pathway in embryonic neural stem cells leads to development of tuberous sclerosis complex-associated lesions.
The significance of fetal ventriculomegaly: etiology, short- and long-term outcomes.
Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.
Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes.
Ethanol inhibition of aspartyl-asparaginyl-beta-hydroxylase in fetal alcohol spectrum disorder: potential link to the impairments in central nervous system neuronal migration.