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467101 to 467200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Acidophil adenomas with intracytoplasmic filamentous aggregates. A light and electron microscopic study.
Absence of chromophobe adenomas from a large series of pituitary tumors.
[Morphogenesis and micromorphology of epithelial tumors of the kidney of nitrosomorpholine intoxicated rats. I. Induction and histology (author's transl)].
Transcranial management of pituitary tumours with suprasellar extension.
Pituitary adenomas: factors in treatment.
Complete Blood Count Abnormal, Doughy Skin, Increased Sweating
Intracranial removal of pituitary adenomas. An evaluation of varying degree of excision from partial to total.
Cerebrospinal fluid hormone concentration in the evaluation of pituitary tumors.
"Nonfunctioning" pituitary tumors: a light and electron microscopical study.
The relationship of time-dose fractionation factors to complications in the treatment of pituitary tumors by irradiation.
Rapid pituitary tumor shrinkage with dissociation between antiproliferative and antisecretory effects of a long-acting octreotide in an acromegalic patient.
HEMORRHAGE INTO PITUITARY ADENOMATA. REPORT OF TWO CASES WITH SPONTANEOUS RECOVERY.
Prolactin and growth hormone in patients with pituitary adenomas: a correlative study of hormone in tumor and plasma by immunoperoxidase technique and radioimmunoassay.
A 2-year dose-response study of lesion sequences during hepatocellular carcinogenesis in the male B6C3F(1) mouse given the drinking water chemical dichloroacetic acid.
cefalee, dureri abdominale, hemoliza, trombocitopenie
Transsphenoidal microsurgery in the treatment of acromegaly and gigantism.
Pierre-Robin syndrome associated with Chiari I malformation.
Lupus erythematosus complicated by the Chiari-Frommel syndrome and autoimmune thyroiditis.
INDUCTION OF OVULATION WITH CLOMIPHENE.
Chiari-Frommel syndrome; a syndrome characterized by galactorrhea, amenorrhea, and pituitary dysfunction; report of two cases.
Chiari-Frommel syndrome in a patient with primary adrenocortical insufficiency.
Abnormal lactation with Cushing's syndrome--a case report.
A successful quintuplet pregnancy following treatment with human pituitary gonadotrophin.
A simple twenty-four hour test to evaluate hypothalamus-pituitary-adrenal cortical function.
Endocrine patterns in the African. Clinico-biochemical assessment.
Prolactin secretion in sixty-five patients with galactorrhea.
Growth hormone in acromegaly: effect of heavy particle pituitary irradiation.
Current concepts in the treatment of anovulation.
A syndrome of primary hypothyroidism, amenorrhea and galactorrhea.
The LH-releasing hormone test in 31 women with secondary amenorrhoea.
Spectrum of nonpuerperal galactorrhea: report of two cases evolving through the various syndromes.
Secretion of prolactin by patients with pituitary and hypothalamic tumors.
Effects of melatonin and serotonin on the release of FSH and prolactin.
Levodopa suppression of prolactin in nonpuerperal galactorrhea.
Limberg flap coverage for axillary defects resulting from excision of hidradenitis suppurativa.
Isotretinoin treatment of acne and related disorders: an update.
Hidradenitis suppurativa of the adult and its management.
Hidradenitis and other variants of acne.
A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene.
muscas and general weakness in arms and chest, facial muscle weakness, weakness
Exercise for vasomotor menopausal symptoms.
Autonomic dysfunction in multiple sclerosis.
A new simple method for assessing sudomotor function: relevance in type 2 diabetes.
Prospective differentiation of multiple system atrophy from Parkinson disease, with and without autonomic failure.
Host-defense mechanisms in hidradenitis suppurativa.
Exercise for vasomotor menopausal symptoms.
Towards a new classification of ectodermal dysplasias.
Evaluation of sudomotor function.
Earwax, osmidrosis, and breast cancer: why does one SNP (538G>A) in the human ABC transporter ABCC11 gene determine earwax type?
Diabetic autonomic neuropathy.
Biology of sweat glands and their disorders. I. Normal sweat gland function.
A frameshift mutation in peroxisome-proliferator-activated receptor-gamma in familial partial lipodystrophy subtype 3 (FPLD3; MIM 604367).
LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance.
Fatty acid metabolism in patients with PPARgamma mutations.
CADASIL: a critical look at a Notch disease.
Peroxisome proliferator-activated receptor-γ mutations responsible for lipodystrophy with severe hypertension activate the cellular renin-angiotensin system.
A new method for body fat evaluation, body adiposity index, is useful in women with familial partial lipodystrophy.
Strategic role of frontal white matter tracts in vascular cognitive impairment: a voxel-based lesion-symptom mapping study in CADASIL.
Muscle and nerve pathology in Dunnigan familial partial lipodystrophy.
Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Genetics of metabolic syndrome: is there a role for phenomics?
muscas and general weakness in arms and chest, facial muscle weakness
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.
Familial partial lipodystrophy phenotype resulting from a single-base mutation in deoxyribonucleic acid-binding domain of peroxisome proliferator-activated receptor-gamma.
Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophy.
Neonatal porencephaly and adult stroke related to mutations in collagen IV A1.
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.
Comparison of efficacy and safety of leptin replacement therapy in moderately and severely hypoleptinemic patients with familial partial lipodystrophy of the Dunnigan variety.
In silico investigation of molecular mechanism of laminopathy caused by a point mutation (R482W) in lamin A/C protein.
Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies.
Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients.
Impaired peroxisome proliferator-activated receptor gamma function through mutation of a conserved salt bridge (R425C) in familial partial lipodystrophy.
Notch signaling, brain development, and human disease.
Resistance to high-fat diet-induced obesity but exacerbated insulin resistance in mice overexpressing preadipocyte factor-1 (Pref-1): a new model of partial lipodystrophy.
Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy.
Long-term efficacy of leptin replacement in patients with Dunnigan-type familial partial lipodystrophy.
Donepezil in patients with subcortical vascular cognitive impairment: a randomised double-blind trial in CADASIL.
Notch and disease: a growing field.
Notch signaling regulates platelet-derived growth factor receptor-beta expression in vascular smooth muscle cells.
Notch signaling in normal and disease States: possible therapies related to glycosylation.
Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease.
Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence.
Notch signaling in blood vessels: who is talking to whom about what?
Notch signaling in vascular development and physiology.
Primary laminopathy fibroblasts display altered genome organization and apoptosis.
Lipodystrophies: disorders of adipose tissue biology.
Anomalous systemic venous connection. Surgical considerations.
Anatomically corrected transposition of the great arteries.
The spectrum of the scimitar syndrome.
Pathologic anatomy of dextrocardia and its clinical implications.
Left lower quadrant pain of unusual cause.
Laparoscopic cholecystectomy in situs inversus totalis.
D-bulboventricular loop with L-transposition in situs inversus.
Complete atrioventricular block in patients with atrioventricular discordance.
The spectrum of common atrioventricular orifice (canal).
Single (primitive) ventricle.
Echographic determination of left ventricular volumes in pediatric patients.