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486101 to 486200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Paraneoplastic pemphigus. An autoimmune mucocutaneous disease associated with neoplasia.
Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosa.
Production of epidermal acantholysis in normal human skin in vitro by the IgG fraction from pemphigus serum.
Desmoglein 3 anchors telogen hair in the follicle.
Novel human alpha9 acetylcholine receptor regulating keratinocyte adhesion is targeted by Pemphigus vulgaris autoimmunity.
Corticosteroid therapy in the neonatal period.
[Successful cortisone therapy of sclerema adiposum neonatorum].
Sclerema neonatorum treated with corticotropin (ACTH) report of two cases.
Sclerema neonatorum: a review of nomenclature, clinical presentation, histological features, differential diagnoses and management.
Sclerema neonatorum successfully treated with corticotropin (ACTH).
Ischemic extremities due to compartment syndromes in a septic neonate.
Fatty crystals in sclerema neonatorum.
Epidemiological study on hypothermia in newborns.
A case of Hutchinson-Gilford progeria syndrome mimicking scleredema in early infancy.
Cortisone in the treatment of sclerema neonatorum.
Sclerema neonatorum: recovery with cortisone.
Radial nerve palsy associated with localized subcutaneous fat necrosis in the newborn.
Predictors of mortality in infants with sclerema presenting to the Centre for Diarrhoeal Disease, Dhaka.
Factors associated with sclerema in infants with diarrhoeal disease: a matched case-control study.
Exchange transfusion in severe neonatal infection with sclerema.
Acute volvulus of the stomach in infants and children.
Care of the seriously ill neonate with hyaline membrane disease and with sepsis (sclerema neonatorum).
Role of exchange transfusion in the treatment of severe septicemia.
Donor age and factors related to endothelial cell loss 10 years after penetrating keratoplasty: Specular Microscopy Ancillary Study.
Descemetic DALK and predescemetic DALK: outcomes in 236 cases of keratoconus.
Coupling of HRT II and AS-OCT to evaluate corneal endothelial cell loss and in vivo visualization of the Ahmed glaucoma valve implant.
Comparison of flex-center, center, and corner methods of corneal endothelial cell analysis.
Efficacy and safety of femtosecond laser-assisted corneal endothelial keratoplasty: a randomized multicenter clinical trial.
Descemet's stripping automated endothelial keratoplasty: three-year graft and endothelial cell survival compared with penetrating keratoplasty.
Baseline factors related to endothelial cell loss following penetrating keratoplasty.
The ROCK inhibitor eye drop accelerates corneal endothelium wound healing.
Optimizing descemet membrane endothelial keratoplasty using intraoperative optical coherence tomography.
Mathematical projection model of visual loss due to fuchs corneal dystrophy.
Long-term results of deep anterior lamellar keratoplasty for the treatment of keratoconus.
Endothelial failure after collagen cross-linking with riboflavin and UV-A: case report with literature review.
Corneal collagen crosslinking in progressive keratoconus: multicenter results from the French National Reference Center for Keratoconus.
Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation.
Descemet's membrane endothelial keratoplasty: prospective study of 1-year visual outcomes, graft survival, and endothelial cell loss.
Descemet stripping automated endothelial keratoplasty with a graft insertion device: surgical technique and early clinical results.
Primary cilia dynamics instruct tissue patterning and repair of corneal endothelium.
Long-term results of deep anterior lamellar versus penetrating keratoplasty.
Corneal collagen cross-linking with riboflavin and ultraviolet-A irradiation in patients with thin corneas.
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis.
Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis.
[A NEW DYSOSTOSIS WITH URINARY ELIMINATION OF CHONDROITIN SULFATE B].
Mechanisms of the anabolic effects of teriparatide on bone: insight from the treatment of a patient with pycnodysostosis.
Decreased bone turnover and deterioration of bone structure in two cases of pycnodysostosis.
Characterization of novel cathepsin K mutations in the pro and mature polypeptide regions causing pycnodysostosis.
Recurrent PRKAR1A mutation in acrodysostosis with hormone resistance.
Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres.
Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis.
Mutated MESP2 causes spondylocostal dysostosis in humans.
Abnormal vertebral segmentation and the notch signaling pathway in man.
Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.
Notch signaling in development and disease.
Notch signaling and inherited disease syndromes.
Dysregulation of chondrogenesis in human cleidocranial dysplasia.
Immunoglobulin motif DNA recognition and heterodimerization of the PEBP2/CBF Runt domain.
Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse model.
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
A Runx2 threshold for the cleidocranial dysplasia phenotype.
The developmental control of osteoblast-specific gene expression: role of specific transcription factors and the extracellular matrix environment.
Cleidocranial dysplasia: clinical and molecular genetics.
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.
Cbfa1: a molecular switch in osteoblast biology.
A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia.
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
Genetic diversity assessed by amplified fragment length polymorphism analysis of the parasitic nematode Dictyocaulus viviparus the lungworm of cattle.
Efficacy of avermectin B1a for treatment of experimentally induced nematode infections in cattle.
Calfhood vaccination for dictyocaulosis.
A field survey on the status of internal parasites in calves on organic dairy farms in southwestern Sweden.
The pathology of respiratory diseases of adult cattle in Britain.
Survey of helminth infections in Maine dairy cattle.
Serum immunoglobulin E response in calves infected with the lungworm Dictyocaulus viviparus and its correlation with protection.
Population genetics of the bovine/cattle lungworm (Dictyocaulus viviparus) based on mtDNA and AFLP marker techniques.
Lungworms of ruminants.
Epidemiological investigations on Dictyocaulus viviparus (Bloch, 1782) infection in cattle.
Epidemiology of nematode infections of Soay sheep (Ovis aries L.) on St Kilda.
Assessment of the genetic relationship between Dictyocaulus species from Bos taurus and Cervus elaphus using complete mitochondrial genomic datasets.
Vaccine development and diagnostics of Dictyocaulus viviparus.
Immunological studies on Dictyocaulus viviparus infection; immunity produced by the administration of irradiated larvae.
Arrested development of nematodes and some related phenomena.
Immunological studies on Dictyocaulus viviparus infection: the immunity resulting from experimental infection.
A transcriptomic analysis of the adult stage of the bovine lungworm, Dictyocaulus viviparus.
The epidemiology and control of some nematode infections in grazing animals.
Deep insights into Dictyocaulus viviparus transcriptomes provides unique prospects for new drug targets and disease intervention.
The effect of maternal smoking on respiratory and arousal patterns in preterm infants during sleep.
The role of nematode parasites in Soay sheep (Ovis aries L.) mortality during a population crash.
Rehabilitation is compromised by arousal and sleep disorders: results of a survey of rehabilitation centres.
Nocturnal frontal lobe epilepsy and non-rapid eye movement sleep parasomnias: differences and similarities.