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11,059 Possible Causes for 2, FAMILY,, MEMBER, SPINDLIN

  • Dementia

    In the baseline, a 2-phase procedure for identifying cases and noncases of dementia was implemented. SETTING: Zaragoza, Spain.[ncbi.nlm.nih.gov] Family caregivers of people with dementia, often called the invisible second patients, are critical to the quality of life of the care recipients.[ncbi.nlm.nih.gov] The Chairperson is also an ex-officio member on the Board of Alzheimer Europe with full voting rights.[alzheimer-europe.org] , Queen Wellcome V0013481.jpg 3 204 2 308; 4,19 MB Timeline 2.jpg 1 031 517; 65 KB Title3.PNG 409 346; 50 KB True Life Love Story.jpg 1 762 2 048; 467 KB U.S.[commons.wikimedia.org]

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  • Multiple Endocrine Neoplasia Type 2A

    Multiple endocrine neoplasia type 2 (MEN2) (also known as "Pheochromocytoma and amyloid producing medullary thyroid carcinoma", "PTC syndrome," and "Sipple syndrome") is a[en.wikipedia.org] Our aim was to evaluate the frequency of RET mutation in 10 Saudi families with MEN type 2A and familial MTC.[ncbi.nlm.nih.gov] No mutations in these exons were detected in any unaffected normal members of MEN 2A.[ncbi.nlm.nih.gov] Multiple endocrine neoplasia type 2 is historically composed of three clinical subtypes, all of which are associated with germline mutations in the RET proto-oncogene.[ncbi.nlm.nih.gov]

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  • Influenza

    Single-dose treatments (5 to 40 mg/kg of body weight given intraperitoneally) of ferrets with 2'-deoxy-2'-fluoroguanosine or its prodrug, 2,6-diamino-purine-2'-fluororiboside[ncbi.nlm.nih.gov] The classification of the new virus in a separate genus of the Orthomyxoviridae family is proposed.[doi.org] In communicating with Member States, EISN utilises National Focal Points, who are responsible for overseeing interactions between ECDC and individual Member States regarding[ecdc.europa.eu] DOI: 10.1128/AAC.38.8.1864 ABSTRACT Single-dose treatments (5 to 40 mg/kg of body weight given intraperitoneally) of ferrets with 2'-deoxy-2'-fluoroguanosine or its prodrug[doi.org]

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  • Acute Gastroenteritis

    Abstract The cases of 2 siblings with cat scratch disease are described who presented with symptoms suggestive of acute febrile gastroenteritis.[ncbi.nlm.nih.gov] Lower income families may, rationally, apply a different threshold for seeking treatment than higher income families.[bmjopen.bmj.com] […] village, source of drinking water from well of 'new' Rajpara village, change in taste of water, use of chlorine tablets, travel outside village in last week, another family member[ncbi.nlm.nih.gov] Fu JG 1, 2 , Shi C 3 , Xu C 4 , Lin Q 5 , Zhang J 6 , Yi QH 7 , Zhang J 8 , Bao CJ 2 , Huo X 2 , Zhu YF 4 , Ai J 2 , Xing Z 1, 9 .[ncbi.nlm.nih.gov]

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  • Familial Medullary Thyroid Carcinoma

    Familial cases represent multiple endocrine neoplasia type 2 (MEN 2). What is multiple endocrine neoplasia type 2 (MEN 2)?[stanfordhealthcare.org] Abstract Familial medullary thyroid carcinoma is a distinct clinical entity in which early diagnosis by screening of family members for elevated calcitonin levels can be useful[ncbi.nlm.nih.gov] Basal and pentagastrin-stimulated CT concentrations were measured in 71 healthy volunteers--aged 20-67 years--and 76 genetically unaffected members of families with hereditary[ncbi.nlm.nih.gov] Abstract We studied prospectively 46 members of a kindred with familial medullary thyroid carcinoma to determine the importance of possible cellular immune reactivity to tumor[ncbi.nlm.nih.gov]

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  • Upper Respiratory Infection

    N Engl J Med. 2006 Jan 12;354(2):119–30. German M, Olsha R, Kristjanson E, Marchand-Austin A, Peci A, Winter AL, et al.[wwwnc.cdc.gov] Family physicians and educators are encouraged to reexamine their treatment and teaching practices for the common cold.[ncbi.nlm.nih.gov] The OR were adjusted for other covariates like sex of the child, parents' education, type of house, birth weight, number of family members, passive smoking, use of firewood[ncbi.nlm.nih.gov] Personal exposures to NO(2) were measured with Palmes tubes that were changed weekly.[ncbi.nlm.nih.gov]

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  • Episodic Ataxia

    […] in an EA–2 clinical phenotype.[doi.org] We report a family with affected members who had features of episodic ataxia type II and cerebellar atrophy on MRI imaging.[ncbi.nlm.nih.gov] The clinically affected family members showed recurrent vertigo, interictal nystagmus, and childhood epilepsy.[ncbi.nlm.nih.gov] Given the familial aggregation of migraine and migrainous vertigo, our objective was to identify predisposing genetic factors.[ncbi.nlm.nih.gov]

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  • Osteoporosis

    […] that BMD correlates negatively with BTMs and positively with E 2 and Mg (2 ) levels.[ncbi.nlm.nih.gov] We identified a family with novel WNT1 mutation. The index case, a 6 month old child presented with fractures from early infancy.[ncbi.nlm.nih.gov] The full article is accessible to AMA members and paid subscribers. If you are an AMA member or have a subscription login to read more or purchase a subscription now.[doi.org] Existing Univadis member: Please login to continue Welcome! Great to have you back.[merckmedicus.com]

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  • Pharyngitis

    All children treated with amoxicillin for "strep throat" by 5 PM of day 1 may, if afebrile and improved, attend school on day 2.[ncbi.nlm.nih.gov] Eighteen PFAPA case subjects (23%) had 1 family member with PFAPA.[ncbi.nlm.nih.gov] An online survey assessing diagnostic and treatment approaches was sent to 424 members of the Childhood Arthritis and Rheumatology Research Alliance (CARRA) and 980 members[ncbi.nlm.nih.gov] Drafted recommendations were formulated and then reviewed by the task force members until a final consensus was reached.[ncbi.nlm.nih.gov]

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  • Hereditary Hypophosphatemic Rickets with Hypercalciuria

    Term Browser Genes (2) Models (2) Disease References using Mouse Models (2)[informatics.jax.org] Figure 1 Family pedigree showing the haplotypes and analytical findings .[ojrd.biomedcentral.com] Antibody Gene Names: SLC34A3 ; HHRH; NPTIIc Other Names: sodium-dependent phosphate transport protein 2C; solute carrier family 34 (type II sodium/phosphate cotransporter); member[mybiosource.com] (RV: 43.12 10.21 ), 19µEq/min/1.73m 2 (RV: 63,80 19,54) and 36µEq/min/1,73m 2 (RV: 107.17 28.18 ), respectively (analytical standard of incomplete distal renal tubular acidosis[revistanefrologia.com]

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