Histiocytosis Association
The Histiocytosis Association, a non-profit organization registered with the Federal Government, is dedicated to helping those dealing with the effects of rare histiocytic disorders by providing a variety of educational programs and emotional support services. In addition, the Association promotes examination of histiocytic disorders through scientific and medical research, with the aim of establishing better treatments, a cure, and ultimately, prevention of the diseases.- 29:00
- 21 күн бұрын
Hank from Indiana Full Interview
- 3:11
- 21 күн бұрын
2024 Blue Ribbon Run Team Histio
- 19:38
- 28 күн бұрын
Ambassador Andrea Interview
- 15:00
- Ай бұрын
Meet Ambassador Megan
- 37:18
- Ай бұрын
Ambassador Carol Full Awareness Month Interview
- 18:49
- Ай бұрын
Ambassador Ana Full Awareness Month Interview
- 1:29:34
- Ай бұрын
Nate Awareness Full Interview
- 1:02:46
- 3 ай бұрын
Pulmonary Hypertension in Pulmonary Langerhans cell histiocytosis
- 3:19
- 4 ай бұрын
2024 Scholarship Reaction Compilation
- 21:53
- 6 ай бұрын
Malignant Histiocytosis Pathology Interview
- 17:02
- 6 ай бұрын
ANHL2121 Clinical Trial DayOne Interview
- 25:01
- 7 ай бұрын
Interview on Neurodegeneration in LCH with Dr. Ken McClain, Dr. Carl Allen, and Dr. Jen Picarsic.
- 27:09
- 8 ай бұрын
NEW Danaher-IGI Beacon for CRISPR Cures center and their groundbreaking research into HLH!
- 4:23
- 8 ай бұрын
Dr. Zoref Lorenz Grant Award Summary
- 19:25
- 8 ай бұрын
Dr. Zoref-Lorenz and Dr. Michael Jordan on "Inpatient Recognition and Management of HLH"
- 56:14
- 8 ай бұрын
Bridging the Gap of Bone Marrow Transplant Care:
- 18:16
- 9 ай бұрын
New AVP-D Diagnostic Testing
- 1:03:15
- 9 ай бұрын
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