Search Results - "Armstrong, Linlea"

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Cost-effectiveness of MRI for breast cancer screening in BRCA1/2 mutation carriers.

Authors: Pataky, Reka Armstrong, Linlea Chia, Stephen et al.

Source: BMC Cancer. 2013, Vol. 13 Issue 1, p1-9. 9p. 1 Diagram, 4 Charts, 3 Graphs.

Transforming Primary Care: The Expanding Role of Genomic Medicine Beyond Rare Disease.

Authors: Handra, Julia Shojaei, Delaram Armstrong, Linlea

Source: UBC Medical Journal. Fall2024, Vol. 16 Issue 1, p19-21. 3p.

A girl with developmental delay, ataxia, cranial nerve palsies, severe respiratory problems in infancy-Expanding NDST1 syndrome.

Authors: Armstrong, Linlea Tarailo‐Graovac, Maja Sinclair, Graham et al.

Source: American Journal of Medical Genetics. Part A; Mar2017, Vol. 173 Issue 3, p712-715, 4p

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Bye to burnout: intergenerational narratives break barriers.

Authors: Yoo, Jaeyun Matos, Meghan Bota, Melissa et al.

Source: Medical Education. May2019, Vol. 53 Issue 5, p518-518. 1p.

Subjects: Psychological burnout prevention, Intergenerational relations, Medical personnel, Medical practice, Adult education workshops, Psychosocial factors, Narrative medicine

Perioperative Hypotensive Crisis in an Adolescent with a Pancreatic VIPoma and MEN1-Gene Variant.

Authors: Acosta-Gualandri, Alejandra Kao, Kung-Ting Wong, Tiffany et al.

Source: Hormone Research in Paediatrics. 2019, Vol. 91 Issue 4, p285-289.

Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes.

Authors: Giampietro, Philip F. Armstrong, Linlea Stoddard, Alex et al.

Source: American Journal of Medical Genetics. Part A; Jan2015, Vol. 167A Issue 1, p95-102, 8p

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Severe hypospadias and its association with maternal-placental factors.

Authors: Huisma, Felicity Thomas, Marion Armstrong, Linlea

Source: American Journal of Medical Genetics. Part A; Sep2013, Vol. 161A Issue 9, p2183-2187, 5p

The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case-control study.

Authors: Armstrong, Linlea Jett, Kimberly Birch, Patricia et al.

Source: American Journal of Medical Genetics. Part A; Jul2013, Vol. 161A Issue 7, p1654-1661, 8p

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Cerebrovasculopathy in NF1 associated with ocular and scalp defects.

Authors: Smith, Matt Heran, Manraj K.S. Connolly, Mary B. et al.

Source: American Journal of Medical Genetics. Part A; Feb2011, Vol. 155A Issue 2, p380-385, 6p

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Integrating Genomics into Clinical Practice.

Authors: Armstrong, Linlea¹ llarmstrong@cw.bc.ca

Source: UBC Medical Journal. Feb2013, Vol. 4 Issue 2, p8-9. 2p.

Coaching the coaches: Employing role modeling and coaching as a faculty development strategy.

Authors: Price, Ingrid Hubinette, Maria Armstrong, Linlea et al.

Source: Medical Teacher. Aug2021, Vol. 43 Issue 8, p918-919. 2p.

Subjects: OCCUPATIONAL roles, ROLE models, MENTORING, HUMAN services programs, EDUCATORS, MEDICAL schools, AUTONOMY (Psychology), TEACHER development, MEDICAL education, PERSONNEL management, GOAL (Psychology)

Geographic Terms: CANADA

Expanding the genotype-phenotype spectrum in SCN8A-related disorders.

Authors: Hebbar, Malavika Al-Taweel, Nawaf Gill, Inderpal et al.

Source: BMC Neurology. 1/17/2024, Vol. 24 Issue 1, p1-7. 7p.

Enhancing Patient Care Through Effective Genomic Data Management.

Authors: Hannam-Clark, Stephanie Handra, Julia Alderman, Emily et al.

Source: UBC Medical Journal. Fall2024, Vol. 16 Issue 1, p6-7. 3p.

A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD.

Authors: Lu, Henry Y. Vaseghi-Shanjani, Maryam Lam, Avery J. et al.

Source: Journal of Clinical Immunology. 4/28/2025, Vol. 45 Issue 1, p1-18. 18p.

Case Series: A Kindred With Eruptive Vellus Hair Cysts and Systemic Features.

Authors: Ponzo, Marisa G. Van Allen, Margot I. Armstrong, Linlea et al.

Source: Journal of Cutaneous Medicine & Surgery. Nov/Dec2017, Vol. 21 Issue 6, p564-567. 4p.