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COVID-19 AND VWF
COVID-19 and VWF. Jul 17, 2020. Recently, there has been considerable interest in the role von Willebrand Factor (VWF) may play in the complications of COVID-19, the infection caused by SARS-CoV-2, including in lay online media. The SARS-CoV-2 virus attaches to the cells that line blood vessels and in some people causes a severeinflammatory
COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
MAY 2021 WEDNESDAY WEBINARS May 2021 Wednesday Webinars. Apr 30, 2021. NHF's Wednesday Webinars for May 2021 will focus on Women's Health Month, featuring topics of interest to both patients and healthcare providers who are interested in issues faced by women with inheritable blood disorders. May Webinars. All webinars are from 2:00pm-3:00pm ET. HEMOPHILIA OF IOWA, INC. Get directions. Hemophilia of Iowa, Inc. Hemophilia of Iowa, Inc. 1570 South 1st Avenue #J. Iowa City, IA 52240. United States. RECOMMENDATION ON THE USE AND MANAGEMENT OF … a. FVIIIa has multiple sites of interaction with FIXa, FX and the phospholipid surface whereas emicizumab binds to single sites withinFIX(a) and FX(a)
BDC 2021
BDC 2021 will be fully virtual. This will enable us to help ensure the health and safety of all our participants. If playback doesn't begin shortly, try restarting your device. Videos you watch may be added to the TV's watch history and influence TV recommendations. To avoid this, cancel and sign in to YouTube on your computer. MASAC RECOMMENDATIONS REGARDING STANDARDS OF … masac document #188 (replaces #181) masac recommendations regarding standards of service for pharmacy providers of clotting factor concentrates for home NATIONAL HEMOPHILIA FOUNDATION The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. LEARN MORE ABOUT THE COVID-19 VACCINES AND ITP Learn More About the COVID-19 Vaccines and ITP. Mar 12, 2021. As part of a patient education webinar series known as ITP INSIGHTS SM, the Platelet Disorder Support Association (PDSA) recently recorded a session on the new COVID-19 vaccines and immune thrombocytopenic purpura (ITP), a disorder characterized by low platelet levels. COVID-19 VACCINATION GUIDANCE FOR PEOPLE WITH BLEEDING - 1 - COVID-19 vaccination guidance for people with bleeding disorders Guidance from the World Federation of Hemophilia (WFH), EuropeanAssociation for
COVID-19 AND VWF
COVID-19 and VWF. Jul 17, 2020. Recently, there has been considerable interest in the role von Willebrand Factor (VWF) may play in the complications of COVID-19, the infection caused by SARS-CoV-2, including in lay online media. The SARS-CoV-2 virus attaches to the cells that line blood vessels and in some people causes a severeinflammatory
COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
MAY 2021 WEDNESDAY WEBINARS May 2021 Wednesday Webinars. Apr 30, 2021. NHF's Wednesday Webinars for May 2021 will focus on Women's Health Month, featuring topics of interest to both patients and healthcare providers who are interested in issues faced by women with inheritable blood disorders. May Webinars. All webinars are from 2:00pm-3:00pm ET. HEMOPHILIA OF IOWA, INC. Get directions. Hemophilia of Iowa, Inc. Hemophilia of Iowa, Inc. 1570 South 1st Avenue #J. Iowa City, IA 52240. United States. RECOMMENDATION ON THE USE AND MANAGEMENT OF … a. FVIIIa has multiple sites of interaction with FIXa, FX and the phospholipid surface whereas emicizumab binds to single sites withinFIX(a) and FX(a)
BDC 2021
BDC 2021 will be fully virtual. This will enable us to help ensure the health and safety of all our participants. If playback doesn't begin shortly, try restarting your device. Videos you watch may be added to the TV's watch history and influence TV recommendations. To avoid this, cancel and sign in to YouTube on your computer. MASAC RECOMMENDATIONS REGARDING STANDARDS OF … masac document #188 (replaces #181) masac recommendations regarding standards of service for pharmacy providers of clotting factor concentrates for home NATIONAL HEMOPHILIA FOUNDATION The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research.HEMOPHILIA B
Hemophilia B, also called factor IX (FIX) deficiency or Christmas disease, is a genetic disorder caused by missing or defective factor IX, a clotting protein. Although it is passed down from parents to children, about 1/3 of cases are caused by a spontaneous mutation, a change in a gene. According to the US Centers for Disease Control and HISTORY | NATIONAL HEMOPHILIA FOUNDATION 1926 - Erik von Willebrand identifies a bleeding disorder, later called von Willebrand disease (VWD) 1940s - whole blood transfusions given at hospital. 1948 - National Hemophilia Foundation (NHF) opens as The Hemophilia Foundation, Inc. 1952 - Researchers describe what is now called factor IX clotting protein.GUIDELINES ON CARE
Expert recommendations, statements, and advisories on treatment and care of bleeding disorders. SUPPORT INNOVATIVE RESEARCH With your gift today, you contribute to the development of cures for inheritable blood disorders.GIVE MONTHLY
As a Promise Partner, you demonstrate your commitment to the inheritable blood disorders community through a monthly gift automatically charged to your bank or credit card. Your recurring gift offers dependable support for the services the community relies on.HONOR A LOVED ONE
Honor someone you love with a gift that supports those affected by inheritable blood disorders. Tribute gifts allow you to recognize an individual with a gift made to NHF in their name while ensuring their legacy leaves a lasting impact on the inheritable blood disorderscommunity.
PHYSICAL THERAPY RESOURCES Morgan Johnson. Manager of Healthcare Provider Programs. mail mjohnson@hemophilia.org. phone (212) 328-3745. GENE AND INNOVATIVE THERAPIES EDUCATION We are committed to ensuring people with bleeding disorders understand how gene and innovative therapies work. 2021 TCS NEW YORK CITY MARATHON The National Hemophilia Foundation (NHF) is proud to be an official charity of the 2021 TCS New York City Marathon to take place on Sunday, November 7, 2021.The 26.2-mile New York City Marathon is one of the premiere running events in the world and travels through all five boroughs of New York City. HISTORY | NATIONAL HEMOPHILIA FOUNDATIONSEE MORE ON HEMOPHILIA.ORG COVID-19 VACCINATION GUIDANCE FOR PEOPLE WITH BLEEDING - 1 - COVID-19 vaccination guidance for people with bleeding disorders Guidance from the World Federation of Hemophilia (WFH), EuropeanAssociation for
LEARN MORE ABOUT THE COVID-19 VACCINES AND ITP Learn More About the COVID-19 Vaccines and ITP. Mar 12, 2021. As part of a patient education webinar series known as ITP INSIGHTS SM, the Platelet Disorder Support Association (PDSA) recently recorded a session on the new COVID-19 vaccines and immune thrombocytopenic purpura (ITP), a disorder characterized by low platelet levels.COVID-19 AND VWF
COVID-19 and VWF. Jul 17, 2020. Recently, there has been considerable interest in the role von Willebrand Factor (VWF) may play in the complications of COVID-19, the infection caused by SARS-CoV-2, including in lay online media. The SARS-CoV-2 virus attaches to the cells that line blood vessels and in some people causes a severeinflammatory
COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
MASAC DOCUMENTS
MASAC Documents. NHF’s Medical and Scientific Advisory Council (MASAC) issues recommendations and advisories on treatment, research and other general health concerns for the bleeding disorders community. MASAC communications cover a wide range of medical issues, from prevention and treatment to infectious disease complications andwomen with
PHYSICAL THERAPY RESOURCES Morgan Johnson. Manager of Healthcare Provider Programs. mail mjohnson@hemophilia.org. phone (212) 328-3745. PACIFIC NORTHWEST BLEEDING DISORDERS Pacific Northwest Bleeding Disorders. The Hemophilia Foundation of Oregon enhances the quality of life for individuals with bleeding disorders and their families through advocacy, assistance, outreach, education and research support. Welcome to the Hemophilia Foundation of Oregon! We are primarily a volunteer-run nonprofit organization inOregon.
BDC 2020 - NATIONAL HEMOPHILIA FOUNDATION BDC 2020. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 white-out-section. row-start col-sm-12 bg-white overlap-section border-top border-left border-right border-bottom. row-start col-sm-12 bg-white normal-section padding-left-right. MASAC RECOMMENDATIONS REGARDING STANDARDS OF … masac document #188 (replaces #181) masac recommendations regarding standards of service for pharmacy providers of clotting factor concentrates for home HISTORY | NATIONAL HEMOPHILIA FOUNDATIONSEE MORE ON HEMOPHILIA.ORG COVID-19 VACCINATION GUIDANCE FOR PEOPLE WITH BLEEDING - 1 - COVID-19 vaccination guidance for people with bleeding disorders Guidance from the World Federation of Hemophilia (WFH), EuropeanAssociation for
LEARN MORE ABOUT THE COVID-19 VACCINES AND ITP Learn More About the COVID-19 Vaccines and ITP. Mar 12, 2021. As part of a patient education webinar series known as ITP INSIGHTS SM, the Platelet Disorder Support Association (PDSA) recently recorded a session on the new COVID-19 vaccines and immune thrombocytopenic purpura (ITP), a disorder characterized by low platelet levels.COVID-19 AND VWF
COVID-19 and VWF. Jul 17, 2020. Recently, there has been considerable interest in the role von Willebrand Factor (VWF) may play in the complications of COVID-19, the infection caused by SARS-CoV-2, including in lay online media. The SARS-CoV-2 virus attaches to the cells that line blood vessels and in some people causes a severeinflammatory
COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
MASAC DOCUMENTS
MASAC Documents. NHF’s Medical and Scientific Advisory Council (MASAC) issues recommendations and advisories on treatment, research and other general health concerns for the bleeding disorders community. MASAC communications cover a wide range of medical issues, from prevention and treatment to infectious disease complications andwomen with
PHYSICAL THERAPY RESOURCES Morgan Johnson. Manager of Healthcare Provider Programs. mail mjohnson@hemophilia.org. phone (212) 328-3745. PACIFIC NORTHWEST BLEEDING DISORDERS Pacific Northwest Bleeding Disorders. The Hemophilia Foundation of Oregon enhances the quality of life for individuals with bleeding disorders and their families through advocacy, assistance, outreach, education and research support. Welcome to the Hemophilia Foundation of Oregon! We are primarily a volunteer-run nonprofit organization inOregon.
BDC 2020 - NATIONAL HEMOPHILIA FOUNDATION BDC 2020. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 white-out-section. row-start col-sm-12 bg-white overlap-section border-top border-left border-right border-bottom. row-start col-sm-12 bg-white normal-section padding-left-right. MASAC RECOMMENDATIONS REGARDING STANDARDS OF … masac document #188 (replaces #181) masac recommendations regarding standards of service for pharmacy providers of clotting factor concentrates for home NATIONAL HEMOPHILIA FOUNDATION The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. HISTORY | NATIONAL HEMOPHILIA FOUNDATION 1926 - Erik von Willebrand identifies a bleeding disorder, later called von Willebrand disease (VWD) 1940s - whole blood transfusions given at hospital. 1948 - National Hemophilia Foundation (NHF) opens as The Hemophilia Foundation, Inc. 1952 - Researchers describe what is now called factor IX clotting protein.WEBINARS AND VIDEOS
These educational videos and webinars will help increase your understanding of gene therapy and innovative therapies for hemophilia. COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
FACTOR II | NATIONAL HEMOPHILIA FOUNDATION Factor II (Prothrombin) Deficiency. Factor II (FII) deficiency, also called prothrombin deficiency, was first identified in 1947 by Dr. Armand Quick. The incidence is estimated at 1 in 2 million in the general population. Factor II deficiency is inherited in an autosomal recessive fashion, meaning that both parents must carry the gene topass
FACTOR VII | NATIONAL HEMOPHILIA FOUNDATION Factor VII (FVII), or proconvertin, deficiency was first recognized in 1951. Considered the most common of rare bleeding disorders its incidence is estimated at 1 per 300,000-500,000. It is inherited in an autosomal recessive fashion, meaning both parents must carry the gene to pass it on to their children; it affects men and women equally. GENE AND INNOVATIVE THERAPIES EDUCATION We are committed to ensuring people with bleeding disorders understand how gene and innovative therapies work. MEDICARE | NATIONAL HEMOPHILIA FOUNDATION Medicare is the federal insurance program that provides coverage for the elderly (people aged 65 and older) and people who are disabled. NHF advocates for Medicare policies that benefit the bleeding disorders community in part because Medicare is often seen as the model program that influences coverage by private insurers. 2021 TCS NEW YORK CITY MARATHON The National Hemophilia Foundation (NHF) is proud to be an official charity of the 2021 TCS New York City Marathon to take place on Sunday, November 7, 2021.The 26.2-mile New York City Marathon is one of the premiere running events in the world and travels through all five boroughs of New York City. NHF CONFERENCE & TRAVEL SERVICES National Hemophilia Foundation All rights reserved. HISTORY | NATIONAL HEMOPHILIA FOUNDATIONSEE MORE ON HEMOPHILIA.ORG COVID-19 VACCINATION GUIDANCE FOR PEOPLE WITH BLEEDING - 1 - COVID-19 vaccination guidance for people with bleeding disorders Guidance from the World Federation of Hemophilia (WFH), EuropeanAssociation for
LEARN MORE ABOUT THE COVID-19 VACCINES AND ITP Learn More About the COVID-19 Vaccines and ITP. Mar 12, 2021. As part of a patient education webinar series known as ITP INSIGHTS SM, the Platelet Disorder Support Association (PDSA) recently recorded a session on the new COVID-19 vaccines and immune thrombocytopenic purpura (ITP), a disorder characterized by low platelet levels.COVID-19 AND VWF
COVID-19 and VWF. Jul 17, 2020. Recently, there has been considerable interest in the role von Willebrand Factor (VWF) may play in the complications of COVID-19, the infection caused by SARS-CoV-2, including in lay online media. The SARS-CoV-2 virus attaches to the cells that line blood vessels and in some people causes a severeinflammatory
COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
MASAC DOCUMENTS
MASAC Documents. NHF’s Medical and Scientific Advisory Council (MASAC) issues recommendations and advisories on treatment, research and other general health concerns for the bleeding disorders community. MASAC communications cover a wide range of medical issues, from prevention and treatment to infectious disease complications andwomen with
PHYSICAL THERAPY RESOURCES Morgan Johnson. Manager of Healthcare Provider Programs. mail mjohnson@hemophilia.org. phone (212) 328-3745. PACIFIC NORTHWEST BLEEDING DISORDERS Pacific Northwest Bleeding Disorders. The Hemophilia Foundation of Oregon enhances the quality of life for individuals with bleeding disorders and their families through advocacy, assistance, outreach, education and research support. Welcome to the Hemophilia Foundation of Oregon! We are primarily a volunteer-run nonprofit organization inOregon.
BDC 2020 - NATIONAL HEMOPHILIA FOUNDATIONWORLD HEMOPHILIA FOUNDATIONHEMOPHILIA ORGANIZATIONNATIONAL HEMOPHILIA ASSOCIATIONUNITED HEMOPHILIA FOUNDATIONHEMOPHILIA SYMPTOMSHISTORY OF HEMOPHILIA BDC 2020. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 white-out-section. row-start col-sm-12 bg-white overlap-section border-top border-left border-right border-bottom. row-start col-sm-12 bg-white normal-section padding-left-right. MASAC RECOMMENDATIONS REGARDING STANDARDS OF … masac document #188 (replaces #181) masac recommendations regarding standards of service for pharmacy providers of clotting factor concentrates for home HISTORY | NATIONAL HEMOPHILIA FOUNDATIONSEE MORE ON HEMOPHILIA.ORG COVID-19 VACCINATION GUIDANCE FOR PEOPLE WITH BLEEDING - 1 - COVID-19 vaccination guidance for people with bleeding disorders Guidance from the World Federation of Hemophilia (WFH), EuropeanAssociation for
LEARN MORE ABOUT THE COVID-19 VACCINES AND ITP Learn More About the COVID-19 Vaccines and ITP. Mar 12, 2021. As part of a patient education webinar series known as ITP INSIGHTS SM, the Platelet Disorder Support Association (PDSA) recently recorded a session on the new COVID-19 vaccines and immune thrombocytopenic purpura (ITP), a disorder characterized by low platelet levels.COVID-19 AND VWF
COVID-19 and VWF. Jul 17, 2020. Recently, there has been considerable interest in the role von Willebrand Factor (VWF) may play in the complications of COVID-19, the infection caused by SARS-CoV-2, including in lay online media. The SARS-CoV-2 virus attaches to the cells that line blood vessels and in some people causes a severeinflammatory
COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
MASAC DOCUMENTS
MASAC Documents. NHF’s Medical and Scientific Advisory Council (MASAC) issues recommendations and advisories on treatment, research and other general health concerns for the bleeding disorders community. MASAC communications cover a wide range of medical issues, from prevention and treatment to infectious disease complications andwomen with
PHYSICAL THERAPY RESOURCES Morgan Johnson. Manager of Healthcare Provider Programs. mail mjohnson@hemophilia.org. phone (212) 328-3745. PACIFIC NORTHWEST BLEEDING DISORDERS Pacific Northwest Bleeding Disorders. The Hemophilia Foundation of Oregon enhances the quality of life for individuals with bleeding disorders and their families through advocacy, assistance, outreach, education and research support. Welcome to the Hemophilia Foundation of Oregon! We are primarily a volunteer-run nonprofit organization inOregon.
BDC 2020 - NATIONAL HEMOPHILIA FOUNDATIONWORLD HEMOPHILIA FOUNDATIONHEMOPHILIA ORGANIZATIONNATIONAL HEMOPHILIA ASSOCIATIONUNITED HEMOPHILIA FOUNDATIONHEMOPHILIA SYMPTOMSHISTORY OF HEMOPHILIA BDC 2020. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 cta-section center no-pad. row-start col-sm-12 white-out-section. row-start col-sm-12 bg-white overlap-section border-top border-left border-right border-bottom. row-start col-sm-12 bg-white normal-section padding-left-right. MASAC RECOMMENDATIONS REGARDING STANDARDS OF … masac document #188 (replaces #181) masac recommendations regarding standards of service for pharmacy providers of clotting factor concentrates for home NATIONAL HEMOPHILIA FOUNDATION The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. HISTORY | NATIONAL HEMOPHILIA FOUNDATION 1926 - Erik von Willebrand identifies a bleeding disorder, later called von Willebrand disease (VWD) 1940s - whole blood transfusions given at hospital. 1948 - National Hemophilia Foundation (NHF) opens as The Hemophilia Foundation, Inc. 1952 - Researchers describe what is now called factor IX clotting protein. COVID-19 VACCINES AND BLEEDING DISORDERS: FREQUENTLY ASKED NHF recognizes that people with bleeding disorders may have questions and concerns related to the variant coronavirus’ causing COVID-19 and the new COVID-19 vaccines, including any implications specific totheir conditions.
WEBINARS AND VIDEOS
These educational videos and webinars will help increase your understanding of gene therapy and innovative therapies for hemophilia. MAY 2021 WEDNESDAY WEBINARS May 2021 Wednesday Webinars. Apr 30, 2021. NHF's Wednesday Webinars for May 2021 will focus on Women's Health Month, featuring topics of interest to both patients and healthcare providers who are interested in issues faced by women with inheritable blood disorders. May Webinars. All webinars are from 2:00pm-3:00pm ET. FACTOR II | NATIONAL HEMOPHILIA FOUNDATION Factor II (Prothrombin) Deficiency. Factor II (FII) deficiency, also called prothrombin deficiency, was first identified in 1947 by Dr. Armand Quick. The incidence is estimated at 1 in 2 million in the general population. Factor II deficiency is inherited in an autosomal recessive fashion, meaning that both parents must carry the gene topass
NEWSLETTER ARCHIVE
NHF Health & Wellness eNewsletter – 4/9/21 – Vaccine News & More NHF Health & Wellness eNewsletter – 2/23/21 – Double Masking & Herd Immunity NHF Health & Wellness eNewsletter – 1/11/21 - COVID-19 Vaccine FAQs NHF Health & Wellness eNewsletter – 12/4/20 - Physician Commentary NHF Health & Wellness eNewsletter – 10/30/20 – Long-term COVID-19 Cases FACTOR VII | NATIONAL HEMOPHILIA FOUNDATION Factor VII (FVII), or proconvertin, deficiency was first recognized in 1951. Considered the most common of rare bleeding disorders its incidence is estimated at 1 per 300,000-500,000. It is inherited in an autosomal recessive fashion, meaning both parents must carry the gene to pass it on to their children; it affects men and women equally. MEDICARE | NATIONAL HEMOPHILIA FOUNDATION Medicare is the federal insurance program that provides coverage for the elderly (people aged 65 and older) and people who are disabled. NHF advocates for Medicare policies that benefit the bleeding disorders community in part because Medicare is often seen as the model program that influences coverage by private insurers.HOME PAGE ENGLISH
Games and Interactive Learning Tools. These games and tools were designed to test your understanding and expand your knowledge of bleeding disorders — all in a fun way, of course. Downloadable Checklists, and Information Materials. The information you need to know to help stay safe, healthy, and happy. Skip to main content*
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* RED TIE SOIREE
Please join us for the evening as we pay tribute to the work and achievements of these awardees.Read More* UNITE YOUR WAY
Start your own fundraiser for NHF. Whenever, wherever, however you want. Click here!Read More* NHF'S 71ST BDC
NHF’s 71st Bleeding Disorders Conference will be held October 3 - October 5, 2019 in Anaheim, California. Register Today!Read MoreFEATURED
*
BAYER
RELEASES NEW STATEMENT ON KOGENATE FS RECALL Bayer has responded to NHF's and HFA's queries regarding the recall.*
MEET THE RED
TIE RUNNERS!
Meet the team who are dedicating their 26-mile run to NHF.*
BAYER
RESPONDS TO NHF-HFA JOINT STATEMENT Bayer has responded to NHF and HFA's questions about the recall ofKogenate® FS.
*
FREELINE
PROVIDES UPDATES ON HEMOPHILIA GENE THERAPY PROGRAMS The company is developing gene therapies for both hemophilia A and B, and for several other chronic conditions.*
JOINT
STATEMENT ON RECALL OF BAYER KOGENATE® FS LOTS NHF and HFA submitted a letter to Bayer requesting more informationabout the recall.
*
INVESTIGATORS
REPORT PROGRESS ON NEW SUBCUTANEOUS THERAPY Concizumab is being investigated for the prevention of bleeding episodes in hemophilia A patients, and in hemophilia A/B patients withinhibitors.
*
CASEBIA
PRESENTS DUAL APPROACH TO GENE THERAPY Both AAV vectors _and_ genome editing novel technologies are being brought to bear in this unique and experimental gene therapy.*
SANOFI
PRESENTS FINAL TRIAL DATA FOR RFVIII CANDIDATE The data presented at ISTH reflected marked improvements in FVIII half-life amongst study participants. LIVING WITH A BLEEDING DISORDER Welcome to the Genetics of Bleeding Disorders Types of Bleeding DisordersInhibitors
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YOUR LOCAL CHAPTER!
Find a HEMOPHILIA TREATMENT CENTER Near You! View MASAC's TreatmentRecommendations!
SENSIBLE DIETING CAN HELP YOUR OVERALL HEALTH DRINKING AND BLEEDING DISORDERS WHAT’S THE DEAL WITH CBD OIL? 20 SCREEN-FREE SUMMER ACTIVITIES FOR KIDS WITH BLEEDING DISORDERS BLEEDING DISORDERS IN PREGNANCYTWITTER BLOCK
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