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Academic Journal

Osteomalacia as a Complication of Intravenous Iron Infusion:A Systematic Review of Case Reports

Subjects: FGF-23; FRACTURES; HYPOPHOSPHATEMIA

  • Source: Vilaca , T , Velmurugan , N , Smith , C , Abrahamsen , B & Eastell , R 2022 , ' Osteomalacia as a Complication of Intravenous Iron Infusion : A Systematic Review of Case Reports ' , Journal of Bone

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Academic Journal

Suspicion, screening, and diagnosis of wild-type transthyretin amyloid cardiomyopathy:a systematic literature review

Subjects: Amyloidosis; ATTRwt CM; Cardiomyopathy

  • Source: Bay , K , Gustafsson , F , Maiborg , M , Bagger-Bahnsen , A , Strand , A M , Pilgaard , T & Poulsen , S H 2022 , ' Suspicion, screening, and diagnosis of wild-type transthyretin amyloid cardiomyopathy

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Academic Journal

Family history of psychiatric disorders as a risk factor for maternal postpartum depression: a systematic review protocol

Subjects: Depression; Post partum; pregnancy

  • Source: Zacher Kjeldsen , M-M , Bricca , A , Liu , X , G. Frokjaer , V , Madsen , K B & Munk-Olsen , T 2022 , ' Family history of psychiatric disorders as a risk factor for maternal postpartum depression: a

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Academic Journal

Differences between familial and sporadic dilated cardiomyopathy:ESC EORP Cardiomyopathy & Myocarditis registry

Subjects: Dilated cardiomyopathy; Europe; Familial

  • Source: Asselbergs , F W , Sammani , A , Elliott , P , Gimeno , J R , Tavazzi , L , Tendera , M , Kaski , J P , Maggioni , A P , Rubis , P P , Jurcut , R , Heliö , T , Calò , L , Sinagra , G , Zdravkovic ,

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Academic Journal

Cutaneous Expression of Familial Cancer Syndromes

Subjects: cutaneous lesions; familial cancer; genetic predisposition

  • Source: Andersen , A J , Schierbeck , J , Bygum , A & Puente-Pablo , N 2021 , ' Cutaneous Expression of Familial Cancer Syndromes ' , Acta Dermato-Venereologica , vol. 101 , no.

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Academic Journal

Epilepsy syndromes in the first year of life and usefulness of genetic testing for precision therapy

Subjects: Benign and self-limiting (familial) epilepsy syndromes; Diagnostic yield; Early-onset epilepsy

  • Source: Bayat , A , Bayat , M , Rubboli , G & Møller , R S 2021 , ' Epilepsy syndromes in the first year of life and usefulness of genetic testing for precision therapy ' , Genes , vol. 12 , no. 7 , 1051 .

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Academic Journal

Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients

Subjects: cancer genes; familial pancreatic cancer; first-degree relatives

  • Source: Tan , M , Brusgaard , K , Gerdes , A-M A , Mortensen , M B , Detlefsen , S , Schaffalitzky , O B & Jørgensen , M T 2021 , ' Whole genome sequencing identifies rare germline variants enriched in

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Academic Journal

Familial risk and heritability of hematologic malignancies in the nordic twin study of cancer

Subjects: Biometric modelling; Cumulative risk; Familial risk

  • Source: Clemmensen , S B , Harris , J R , Mengel-From , J , Bonat , W H , Frederiksen , H , Kaprio , J & Hjelmborg , J V B 2021 , ' Familial risk and heritability of hematologic

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Academic Journal

Interaction between Parkin and α-Synuclein in PARK2-Mediated Parkinson's Disease

Subjects: familial Parkinson’s disease; Lewy bodies; PARK2

  • Source: Madsen , D A , Schmidt , S I , Blaabjerg , M & Meyer , M 2021 , ' Interaction between Parkin and α-Synuclein in PARK2-Mediated Parkinson's Disease ' , Cells , vol. 10 , no. 2 , 283 .

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Academic Journal

The phenotypic spectrum of prrt2-associated paroxysmal neurologic disorders in childhood

Subjects: BFIS; Familial infantile epilepsy; Hemiplegic migraine

  • Source: Döring , J H , Saffari , A , Bast , T , Brockmann , K , Ehrhardt , L , Fazeli , W , Janzarik , W G , Kluger , G , Muhle , H , Møller , R S , Platzer , K , Santos , J L , Bache , I , Bertsche , A ,

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