INTERIUM-PHOTOS

Front Line Genomics highlights the Smith Family Clinic for Genomic Medicine

The Smith Family Clinic for Genomic Medicine was featured in a new series from Front Line Genomics, “Digital DNA,” which explores the role of large-scale genetic testing in science, industry and society. David Bick, MD, discussed how the Smith Family Clinic uses the power of genomics to diagnose patients with rare diseases. “We think the
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Baylor University student spends time at Smith Family Clinic during genomic counseling rotation

The HudsonAlpha Institute for Biotechnology offers a two-week summer mini-rotation for genetic counseling students across the U.S. Stacey Edwards, a student at Baylor University, was selected to spend two weeks working alongside the genetic counseling team at HudsonAlpha. We sat down with Stacey to learn more about her experience this summer. Why did you apply
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David Bick called to help update standards for clinical genomic interpretation

Smith Family Clinic geneticist David Bick, MD, FACMG, along with HudsonAlpha Faculty Investigator Elaine Lyon, PhD, FACMG, will participate in the American College of Medical Genetics (ACMG) working group to update standards for interpreting genetic sequence variants test results in a clinical setting. Bick and Lyon participated in creating the first set of standards for variant interpretation, and now
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Hero Fund highlight: Alabama woman ends 40-year diagnostic odyssey, thanks to Smith Family Clinic

Rare disease patients spend an average of eight years searching for a diagnosis, and for some, that search can last decades. April Hudson of Quinton, Ala., began showing symptoms of an unknown disease at three years old. She would go on to see 200 physicians before finally learning the true cause of her symptoms nearly
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Hero Fund highlight: Online search helps solve 24-year medical mystery

Confusion, nausea, fever, anger, then back to normal. This was Lauren Vandiver’s life beginning in early childhood. Her parents, Phillip and Angela Vandiver, spent more than twenty years asking the question “why?” Why is she forgetting who we are? Why is she throwing up? Why is she so angry? They knew there had to be
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Alabama Rare to host FREE patient/caregiver symposium March 2

The 2nd annual Alabama Rare Disease Patient/Caregiver Symposium will take place March 2, 2019 in Birmingham, Ala.  At this free symposium, presented by Alabama Rare, Children’s of Alabama, Rare Disease Day and UAB Medicine, attendees will break down the process of diagnosing a genetic and non-genetic rare disease; discuss what is involved in finding approved and
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Smith Family Clinic administrator selected for Practice Management Association executive committee

Huntsville, Ala. – The Smith Family Clinic for Genomic Medicine – a genomics medical office on the campus of the HudsonAlpha Institute for Biotechnology  – announced today that Carol Aiken, CMM, clinical operations administrator and privacy and compliance officer; was appointed to the Alabama chapter of the American Academy of Pediatrics Practice Management Association (AAP-PMA) executive
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David Bick invited to present at Concierge Medicine Forum

David Bick, MD, has been invited to present at the Concierge Medicine Forum in Atlanta October 26-27. The two-day forum will address current trends that are having an impact on the quality of health care today. Bick will present during the Friday breakout session at 10 am and discuss how genomics can help identify undiagnosed and misdiagnosed
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Meet Veronica Greve, Smith Family Clinic’s newest genetic counselor

Describing her counseling style as calm and understanding, Veronica Greve looks forward to her new role at the HudsonAlpha Institute for Biotechnology and the Smith Family Clinic for Genomic Medicine as a genetic counselor. Greve was initially pursuing a career in plant science but decided she wanted a job where she could see the direct impact of
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David Bick selected to Alabama Rare Disease Advisory Council

Patient diagnoses, treatments, access to care discussed at inaugural meeting David Bick, MD, has been selected by Governor Kay Ivey to serve on the newly-created Alabama Rare Disease Council. The council held its inaugural meeting August 27, 2018 in Birmingham. Bick, who sees rare disease patients at the Smith Family Clinic for Genomic Medicine, brings
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