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Study: Air Pollution Linked To Higher Risk Of Dementia

Algodystrophy
Alzheimer's disease
Angiopathy
Aphasia
Ataxia-telangiectasia
Autosomal dominant cerebellar ataxia
Autosomal recessive cerebellar ataxia
Cephalalgia
Chordoma
Cluster headache
Concussion
Corpus callosum agenesis
Corticobasal degeneration
Cutis verticis gyrata
Dentatorubral pallidoluysian atrophy
Dysautonomia
Dystonia
Encephalitis
Familial dysautonomia
Fanconi anemia
Friedreich ataxia
Harding ataxia
Herpetic encephalitis
Idiopathic aplastic anemia
Late infantile neuronal ceroid lipofuscinosis
Lewy Body Dementia
Multiple system atrophy
Neuronal ceroid lipofuscinosis
Paroxysmal non-kinesigenic dyskinesia
Pelvic and perineal pains
Spinocerebellar ataxia
Spinocerebellar ataxia type 2
Spinocerebellar ataxia type 3
Viral encephalitis
X-linked cerebral adrenoleukodystrophy

Study: Air Pollution Linked To Higher Risk Of Dementia

Alzheimer's Day is this Friday: September, 21 2018If you or a loved one is diagnosed with dementia, join the group and forum here.  Urban air pollution, mostly from vehicles, is associated with an...

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Olivia Newton-John Opens Up On Her Cancer 'Mission' (Diagnosed For Third Time)

Bladder cancer
Brain tumor
Breast cancer
Cancer
Cancer of the Pleura
Cancer of the vulva
Cervical cancer
Colon cancer
Colorectal cancer
Endocrine cancer
Endometrial cancer
Esophageal cancer
Gallbladder cancer
Gastric cancer
Gastrointestinal stromal tumor
Larynx cancer
Leiomyosarcoma
Liver cancer
Neuroendocrine liver cancer
Neuroendocrine tumor
Ovarian cancer
Pancreatic cancer
Prostate cancer
Small cell lung cancer
Testicular cancer
Thymus cancer
Thyroid Cancer

Olivia Newton-John Opens Up On Her Cancer 'Mission' (Diagnosed For Third Time)

Singer and actress Olivia Newton-John has opened up about a third diagnosis for cancer, saying she believed she would "win over it". The Grease star, 69, told Australian TV show Sunday Night she was...

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US Approves First RNA Interference Drug

3-methylcrotonyl-CoA carboxylase deficiency
Acatalasemia
Aceruloplasminemia
Aciduria
Addison's disease
Adenine phosphoribosyltransferase deficiency
Adrenal insufficiency
Alkaptonuria
Alpha 1-antitrypsin deficiency
Alpha-mannosidosis
Amyloidosis
Androgen insensitivity syndrome
Athyreosis
Bariatric surgery
Bartter syndrome
Berardinelli-Seip congenital lipodystrophy
Biotinidase deficiency
Branching enzyme deficiency
Carbamoylphosphate synthetase deficiency
Carnitine palmitoyl transferase II deficiency
Catecholamine-secreting tumor
Chronic hepatic porphyria
Citrullinemia
Classic homocystinuria
Colchicine poisoning
Congenital adrenal hyperplasia
Congenital disorder of glycosylation
Congenital hypogonadotropic hypogonadism
Congenital isolated thyroxine-binding globulin deficiency
Congenital sucrase-isomaltase deficiency
Craniopharyngioma
Crigler-Najjar syndrome
Cushing syndrome
Cystathioninuria
Cystinosis
Cystinuria
Diabetes insipidus
Erythropoietic protoporphyria
Familial amyloid polyneuropathy
Fluid retention
Fructose-1
6-bisphosphatase deficiency
Galactosemia
Gaucher disease
Gitelman syndrome
Glutaryl-CoA dehydrogenase deficiency
Glycine encephalopathy
Glycogen storage disease type 2
Gout disease
Hartnup syndrome
Histidinemia
Hurler syndrome
Hurler-Scheie syndrome
Hyperargininemia
Hyperlipoproteinemia
Hyperlipoproteinemia type 3
Hyperoxaluria
Hyperparathyroidism
Iminoglycinuria
Isolated congenital hyperinsulinism
Isovaleric acidemia
Krabbe disease
Lemierre syndrome
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Maternally-inherited diabetes and deafness
Medium chain acyl-CoA dehydrogenase deficiency
Metabolic syndrome
Metachromatic leukodystrophy
Methylmalonic acidemia
Mitochondrial cytopathies
Mucolipidosis type 2
Mucopolysaccharidosis
Neonatal diabetes mellitus
Nephrogenic diabetes insipidus
Niemann-Pick disease
Non acquired combined pituitary hormone deficiency
Non-diabetic hypoglycemia
Nutrition / Metabolism / Endocrine glands
Obesity
Oculocerebrorenal syndrome
Ornithine transcarbamylase deficiency
Pelizaeus-Merzbacher disease
Pernicious anemia
Phenylketonuria
Pickwick syndrome
Pituitary adenoma
Pituitary insufficiency
Porphyria
Porphyria cutanea tarda
Progeria
Propionic acidemia
Sandhoff disease
Sarcosinemia
Saturnism
Scheie syndrome
Scurvy
Secondary Adrenal Insufficiency
Severe combined immunodeficiency due to adenosine deaminase deficiency
Sialidosis type 1
Sialidosis type 2
Sjögren-Larsson syndrome
Stiff person syndrome
Tay-Sachs disease
Triple H syndrome
Tyrosinemia type 1
Vitamin B12 deficiency
Vitamin D deficiency
Wilson disease
Wolfram syndrome
Wolman disease
Zollinger-Ellison syndrome

US Approves First RNA Interference Drug

Alnylam’s Onpattro (patisiran) can treat a rare hereditary disease by silencing a specific gene. The first therapy based on RNA interference (RNAi) gene silencing has been approved by the US Food and...

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