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Rafael Reitmayer father of child with Hunter Syndrome shares his experience

Rafael Reitmayer father of child with Hunter Syndrome shares his experience


Interview recorded in Brussels during Rare Disease Day 2011 (Feb 28) as part of a European Symposium on Rare Diseases organised by EURORDIS.
 


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What is Hunter Syndrome? - Also Known as MPS II


This video provides an overview of Hunter syndrome, or mucopolysaccharidosis II (MPS II) -- a serious genetic disorder that primarily affects males. In Hunte...
 

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Early Signs & Symptoms of Hunter Syndrome


This short video describes the early symptoms of Hunter syndrome (MPS II). Symptoms are generally not apparent at birth, but usually start to become noticeab...
 

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Steve Nash and Simon Ibell on Hunter Syndrome


Steve Nash and Simon Ibell ask that Enzyme Replacement Therapy be funded by the Provincial Ministries of Health. To sign the petition go to: http://www.ipeti...
 

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Additional Signs and Symptoms of Hunter Syndrome


This short video shows how Hunter Syndrome signs and symptoms emerge over times. These symptoms may include cardiac/valvular heart disease, short stature, jo...
 

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Melissa Hogan is founder of Saving Case, a patient advocacy group organized to help raise awareness of Hunter Syndrome and to help empower all rare disease a...
 

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Raising Rare Boys - Cure Hunter Syndrome


Hunter Syndrome occurs in 1 in 100000 male births. It's very rare, there is no cure and no treatment that affects the brain and improves cognitive function....
 

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Another PGD story: Hunter syndrome


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Will has Hunter Syndrome.
 

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Funding for Hunter Syndrome on Canada AM


I was interviewed on Canada AM becasue of the interest generated by the video Steve and I made. Thanks to Seamus O'Regan for his interest.
 

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Kids with Hunter Syndrome to perform 'The Nutcracker'


Kaabang-abang na pagtatanghal ang inihahanda ang ABS-CBN Philharmonic Orchestra at ng Philippine Ballet Theatre ngayong papalapit na ang Pasko --- ang "The N...
 

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Diagnosing Hunter Syndrome - ENT Doctors May Be Among the First to Spot MPS II


Dr. David E. Karas, MD, a pediatric otolaryngologist at the Yale-New Haven Hospital, discusses the key role ENTs play in the diagnosis of syndromes like MPS ...
 

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Helping ENTs Diagnose Hunter Syndrome (MPS II)


Paediatric ENTs have a crucial role to play in the early diagnosis of mucopolysaccharidosis II (MPS II), or Hunter syndrome. Adenoidectomy/adenotonsillectomy...
 

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Hunter syndrome, or mucopolysaccharidosis II (MPS II), is a serious genetic disorder that primarily affects males (X-linked recessive). It interferes with th...
 

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2012 Our Journey with Hunter Syndrome


A year in James journey with Hunter Syndrome including his Bone Marrow Transplant at Starship Hospital.
 

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Hunter Syndrome in Focus - Moscow


This video is intended for Russian audiences. Watch a brief video about the Hunter in Focus awareness event in Russia.
 

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A video I made of these amazing kids with Hunter Syndrome!
 

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The Role of Surgeons in Early Diagnosis of Hunter Syndrome (MPS II)


Surgeons may plan an important role in the early diagnosis of Hunter Syndrome (MPS II) and other rare metabolic diseases. Dr. Christina Lampe from the Depart...
 

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Hunter Syndrome Disease Progression in Adolescence


This short video is about the multi-systemic effects of Hunter Syndrome as symptoms progress into adolescence. The progressive symptoms can profoundly effect...
 

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Understanding Hunter Syndrome (MPS II)


This short video is about Hunter syndrome, or mucopolysaccharidosis II (MPS II), a serious genetic disorder that primarily affects males. It interferes with ...
 

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Brief overview of hunter syndrome.
 

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Dr. Odell Biology video project.
 

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Hunter Syndrome - Jeans for Genes


A revolutionary new treatment has had amazing results on a boy from Somerset who suffers with a rare condition which makes walking difficult. BBC October 2007.
 

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Overview of Hunter Syndrome


This video is a combination of other videos on Hunter Syndrome to give viewers an idea of what the disease is and the progress of finding a cure.
 

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Mitina Sneshana , MPS, Hunter Syndrome Association, Russia


(In русский) (in Russian) Mitina was a participant in the European Conference on Rare Diseases (ECRD) Krakow 2010. Mitina is a member of the Hunter Syndrome ...
 

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hunter syndrome YouTube 948ad7e81bc374b6


sa mga gustong tumulong visit: www.psod.org.ph.
 

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2020 Mucopolysaccharidosis II (MPS II) (Hunter Syndrome) Global Clinical Trials Market Analysis


Read more at http://www.rnrmarketresearch.com/mucopolysaccharidosis-ii-mps-ii-hunter-syndrome-global-clinical-trials-review-h2-2014-market-report.html “Mucop...
 

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Saving Case


We created this video in February 2010 to explain Case's symptoms of MPS from birth to diagnosis as well as to give information about Hunter Syndrome and oth...
 

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Cristy Naul, mother of Cyrel, who has Hunter Syndrome


Interview at Tagaytay Highlands.
 

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AIIMS ready to give free symptomatic treatment to Hunter Syndrome patient Arian


 

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Health Minister refers Hunter Syndrome patient Arian's case to AIIMS, assures all help


 

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Living with a rare, deadly Hunter syndrome 12 year old Arian's story


 

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Morbus Hunter diagnostizieren


Morbus Hunter diagnostizieren aus Sicht einer Fachärztin für Hals-Nasen-Ohrenheilkunde. This video is intended for German audiences.
 




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