Search Results

Filter
  • 1-10 of  1,947 results for "Lockhart, E"
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Therapeutic aspects of Connection to Country and cultural landscapes among Aboriginal peoples from the Stolen Generations living in urban NSW, Australia.

  • Authors : Yashadhana A; UNSW Ageing Futures Institute, UNSW Sydney, Australia; Centre for Primary Health Care and Equity, UNSW Sydney, Australia

Subjects: Australian Aboriginal and Torres Strait Islander Peoples* ; Health Services, Indigenous*; Female

  • Source: Public health research & practice [Public Health Res Pract] 2023 Dec 06; Vol. 33 (4). Date of Electronic Publication: 2023 Dec 06.Publisher: Sax Institute Country of Publication: Australia NLM ID: 101648133 Publication Model: Electronic Cited Medium:

Record details

×
Academic Journal

Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25.

  • Authors : Barbier M; Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Bahlo M

Subjects: Cerebellar Ataxia* ; Interferon Type I*/Interferon Type I*/Interferon Type I*/genetics ; Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/genetics Spinocerebellar ataxia 25

  • Source: Annals of neurology [Ann Neurol] 2022 Jul; Vol. 92 (1), pp. 122-137. Date of Electronic Publication: 2022 May 07.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.

  • Authors : Stark Z; Australian Genomics, Murdoch Children's Research Institute, Melbourne, VIC, Australia; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia

Subjects: Genomics* ; Health Policy*; Humans

  • Source: American journal of human genetics [Am J Hum Genet] 2023 Mar 02; Vol. 110 (3), pp. 419-426.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print Cited Medium: Internet ISSN: 1537-6605

Record details

×
Academic Journal

An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14.

  • Authors : Rafehi H; Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia; Department of Medical Biology, University of Melbourne, Parkville, VIC, Australia.

Subjects: Cerebellar Ataxia*/Cerebellar Ataxia*/Cerebellar Ataxia*/genetics ; Friedreich Ataxia*/Friedreich Ataxia*/Friedreich Ataxia*/genetics ; Trinucleotide Repeat Expansion*/Trinucleotide Repeat Expansion*/Trinucleotide Repeat Expansion*/genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2023 Jan 05; Vol. 110 (1), pp. 105-119. Date of Electronic Publication: 2022 Dec 08.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

Nosocomial COVID-19 infection in the era of vaccination and antiviral therapy.

  • Authors : McNeil T; Microbiology and Infectious Diseases, Flinders Medical Centre, Adelaide, South Australia, Australia.; College of Medicine and Public Health, Flinders University, Adelaide, South Australia, Australia.

Subjects: COVID-19* ; Cross Infection*/Cross Infection*/Cross Infection*/drug therapy; Humans SARS-CoV-2 variants

  • Source: Internal medicine journal [Intern Med J] 2024 Mar; Vol. 54 (3), pp. 374-381. Date of Electronic Publication: 2023 Nov 27.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 101092952 Publication Model: Print-Electronic

Record details

×
  • 1-10 of  1,947 results for "Lockhart, E"