<--- Back to Details
First PageDocument Content
Rare diseases / Hurler syndrome / Syndromes / Lysosomal storage disease / Mucopolysaccharidosis / Iduronidase / Coarse facial features / Hematopoietic stem cell transplantation / Newborn screening / Health / Medicine / Biology
Rare diseases
Hurler syndrome
Syndromes
Lysosomal storage disease
Mucopolysaccharidosis
Iduronidase
Coarse facial features
Hematopoietic stem cell transplantation
Newborn screening
Health
Medicine
Biology

Newborn Screening for MPS I: Final Report from the Condition Review Workgroup Alex R. Kemper, MD, MPH, MS February 13, 2015

Add to Reading List

Source URL: www.hrsa.gov

Download Document from Source Website

File Size: 1.012,82 KB

Share Document on Facebook

Similar Documents

MUCOPOLYSACCHARIDOSES  Rare Diseases Unit of the Finnish Association of People with Physical Disabilities  Support for this guide was provided by Genzyme.

MUCOPOLYSACCHARIDOSES Rare Diseases Unit of the Finnish Association of People with Physical Disabilities Support for this guide was provided by Genzyme.

DocID: 1fJSQ - View Document

Microsoft Word - Apjohn Ventures Fund 2Q10 Letter Final

Microsoft Word - Apjohn Ventures Fund 2Q10 Letter Final

DocID: 19Qom - View Document

Newborn Screening for MPS I: Final Report from the Condition Review Workgroup Alex R. Kemper, MD, MPH, MS February 13, 2015

Newborn Screening for MPS I: Final Report from the Condition Review Workgroup Alex R. Kemper, MD, MPH, MS February 13, 2015

DocID: 12Amr - View Document

Newborn Screening for MPS 1: Interim Report from the Condition Review Workgroup Alex R. Kemper, MD, MPH, MS September 11, 2014

Newborn Screening for MPS 1: Interim Report from the Condition Review Workgroup Alex R. Kemper, MD, MPH, MS September 11, 2014

DocID: 12qNp - View Document

Review - Laronidase (Aldurazyme)

Review - Laronidase (Aldurazyme)

DocID: FSLw - View Document