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Hypoglycemia
... levels suggest hyperinsulinism or fatty acid oxidation disorder Beta-hydroxybutyrate : should be high during fasting ... levels suggest hyperinsulinism or fatty acid oxidation disorder Free fatty acids: should be high during ... with low ketones suggests fatty acid oxidation disorder Lactic acid: high levels suggest sepsis or ... hypopituitarism or malnutrition Acylglycine : elevation suggests a disorder of fatty acid oxidation Epinephrine: should be ... breast milk or condition interfering with feeding) Congenital hypopituitarism Congenital hyperinsulinism, several types, both ...
http://en.wikipedia.org/wiki/Hypoglycemia - 65k - Cached - Similar pages

Hypoglycemia (Psychology wiki)
... levels suggest hyperinsulinism or fatty acid oxidation disorder Beta-hydroxybutyrate : should be high during fasting ... levels suggest hyperinsulinism or fatty acid oxidation disorder Free fatty acids : should be high during ... with low ketones suggests fatty acid oxidation disorder Lactic acid : high levels suggest sepsis or ... hypopituitarism or malnutrition Acylglycine : elevation suggests a disorder of fatty acid oxidation Epinephrine: should be ... breast milk or condition interfering with feeding) Congenital hypopituitarism Congenital hyperinsulinism , several types, both ...
http://psychology.wikia.com/wiki/Hypoglycemia - 67k - Cached - Similar pages

Myotonic dystrophy
... dystrophy. It is an autosomal dominant genetic disorder affecting one in 8,000 individuals. Onset ... affected individuals is typically six decades. A congenital form of DM can occur in second ... also known as proximal myotonic myopathy (PROMM) Congenital myotonic dystrophy (CMyD) DM1 and DM2 have ... into three overlapping phenotypes - mild, classical and congenital (CMyD). Mild DM Individuals affected with the ... and be unaware that they have the disorder. If they note muscle weakness or ...
http://en.wikipedia.org/wiki/Myotonic_dystrophy - 29k - Cached - Similar pages

List of diseases starting with A
... polyneuritis Acute intermittent porphyria Acute lymphoblastic leukemia congenital sporadic aniridia Acute lymphoblastic leukemia Acute lymphocytic ... crisis Adrenal adenoma, familial Adrenal cancer Adrenal disorder Adrenal gland hyperfunction Adrenal gland hypofunction Adrenal hyperplasia, congenital Adrenal hyperplasia Adrenal hypertension Adrenal hypoplasia congenital, X-linked Adrenal hypoplasia Adrenal incidentaloma Adrenal ... oligophrenia syndrome of Moynahan Alopecia hypogonadism extrapyramidal disorder Alopecia immunodeficiency Alopecia macular degeneration growth ...
http://en.wikipedia.org/wiki/List_of_diseases_starting_with_A - 36k - Cached - Similar pages

Hypotonia
Hypotonia Congenital hypotonia [[Image:{{{Image}}}|190px|center|]] {{{Caption}}} ICD ... strength. Hypotonia is not a specific medical disorder, but a potential manifestation of many different ... gravis poliomyelitis Prader-Willi syndrome kernicterus meningitis congenital cerebellar ataxia encephalitis Werdnig-Hoffman disease myotonic ... trisomy 13 sepsis Aicardi syndrome Canavan disease congenital hypothyroidism hypervitaminosis D Krabbe disease Menkes syndrome ... is actually a symptom of some underlying disorder, it can be difficult to determine ...
http://en.wikipedia.org/wiki/Hypotonia - 26k - Cached - Similar pages

List of diseases starting with H
... syndrome He Hea-Hei Headache, cluster Hearing disorder Hearing impairment Hearing loss Heart aneurysm Heart ... familial Heart block Heart defect round face congenital retarded development Heart defect tongue hamartoma polysyndactyly ... Hemangioma Hemangiomatosis, familial pulmonary capillary Hemangiopericytoma Hemeralopia, congenital essential Hemeralopia, familial Hemi 3 syndrome Hemifacial ... Hereditary elliptocytosis Hereditary fructose intolerance Hereditary hearing disorder Hereditary hearing loss Hereditary hemochromatosis Hereditary hemorrhagic ... Hereditary paroxysmal cerebral ataxia Hereditary peripheral nervous disorder Hereditary primary Fanconi disease Hereditary resistance ...
http://en.wikipedia.org/wiki/List_of_diseases_starting_with_H - 34k - Cached - Similar pages

Psychopathy
Psychopathy Dissocial personality disorder [[Image:{{{Image}}}|190px|center|]] {{{Caption}}} ICD-10 ... is defined in psychiatry as a personality disorder characterised by lack of empathy or conscience ... is most strongly correlated with antisocial personality disorder and the ICD-10 dissocial disorder. It is hoped that the projected DSM ... existence in any person of such hereditary, congenital or acquired condition affecting the emotional ...
http://en.wikipedia.org/wiki/Psychopathy - 27k - Cached - Similar pages

List of diseases starting with M
... Macular degeneration Macular dystrophy, vitelliform Macules hereditary congenital hypopigmented and hyperpigmented Mad-Mag Mad cow ... Mari-Mart Marie type ataxia Marie Unna congenital hypotrichosis Marinesco Sjogren like syndrome Marinesco-Sjogren ... type Mesothelioma Met Meta Metabolic acidosis Metabolic disorder Metabolic Syndrome X Metacarpals 4 and 5 ... Microcephaly, primary autosomal recessive Microcephaly Microco Microcoria, congenital Microcornea corectopia macular hypoplasia Microcornea glaucoma absent ... Minkowski-Chauffard disease Minoxidil antenatal infection Miosis, congenital Mirror hands feet nasal defects Mirror ...
http://en.wikipedia.org/wiki/List_of_diseases_starting_with_M - 47k - Cached - Similar pages

Psychopathy (Psychology wiki)
... is defined in psychiatry as a personality disorder characterised by lack of empathy or conscience ... is most strongly correlated with antisocial personality disorder and the ICD-10 dissocial disorder. It is hoped that the projected DSM ... existence in any person of such hereditary, congenital or acquired condition affecting the emotional or ... to be sentenced by the courts. "Psychopathic Disorder" is legally defined in the The ...
http://psychology.wikia.com/wiki/Psychopathy - 28k - Cached - Similar pages

Genetic testing
... of developing or passing on a genetic disorder. Several hundred genetic tests are currently in ... some anomaly that flags a disease or disorder. The DNA change can be relatively large ... currently test infants for phenylketonuria (a genetic disorder that causes mental retardation if left untreated) and congenital hypothyroidism (a disorder of the thyroid gland). Some states ...
http://en.wikipedia.org/wiki/Genetic_testing - 25k - Cached - Similar pages

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