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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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Overview of Hunter Syndrome


 

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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 (MPS II)


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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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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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


Kendra Lesta tells Norah O'Donnell about losing her son Christopher to a rare disease and why she did PGD to prevent passing it on again. Watch Norah O'Donne...
 

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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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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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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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Will - Hunter Syndrome


Will has Hunter Syndrome.
 

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

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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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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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Brief overview of hunter syndrome.
 

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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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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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Dr. Odell Biology video project.
 

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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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JSB Market Research: Hunter Syndrome Therapeutics


The industry analysis specialist, has released its new report, “Hunter Syndrome Therapeutics - Pipeline Assessment and Market Forecasts to 2019”. The report ...
 

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Cristy Naul, mother of Cyrel, who has Hunter Syndrome


Interview at Tagaytay Highlands.
 

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Hunter Syndrome DeAnna Berar


 

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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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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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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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HSRC celebrates World Rare Disease Day - February 28


Hunter Syndrome Research Coalition celebrates World Rare Disease Day on February 28th by raising awareness of Hunter Syndrome and the challenges faced by fam...
 

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Morbus Hunter diagnostizieren - Dr. Christina Lampe


Diagnose des Morbus Hunter (auch Mukopolysaccharidose Typ II genannt) durch eine Facharzt der Kinder-Chirurgie This video is intended for German audiences.
 

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Zayda (Hunter) has CKS (Crazy Kitten Syndrome) (Adorable Cute Kitten)


Yes Zayda and Vega both have this. Crazy Kitten Syndrome effects many. Some signs that your kitten might have it: 1. Random Violence towards Inanimate Object...
 

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Fragile X Syndrome - Speech Therapy - Hunter Parrish - January 2007


My son, Hunter Parrish, in speech therapy (ST) January 2007. His Speech Therapist from the Anchorage School District attended a private ST session and videot...
 




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