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Multiple Sclerosis (Houndmills, Basingstoke, England)
|
December 8, 2009
Very long chain fatty acid levels in patients diagnosed with multiple sclerosis
Alastair Wilkins, Gillian Ingram, Anny Brown, et al.
Case Reports in Radiology
|
January 10, 2015
Lobar Collapse and Obliteration of Air Bronchogram Allowing Early Diagnosis of Endobronchial Aspergillus Infection following Hematopoietic Stem Cell Transplantation
Elizabeth Thompson, Manigandan S Thyagarajan, Elizabeth Johnson, et al.
Pediatric Transplantation
|
August 24, 2012
Successful cord blood transplantation in a patient with malignant infantile osteopetrosis and hemophilia
David Buchbinder, Colin G Steward, Geetha Puthenveetil, et al.
Journal of Inherited Metabolic Disease
|
October 31, 2012
Diagnosis of Barth syndrome using a novel LC-MS/MS method for leukocyte cardiolipin analysis
Ann Bowron, Robert Frost, Vicki E C Powers, et al.
Journal of Pediatric Orthopedics. Part B
|
May 14, 2015
A severe systemic presentation of pigmented villonodular synovitis in a child with underlying Chediak-Higashi syndrome
Victoria L True, Fergal P Monsell, Tanya A Smith, et al.
British Journal of Haematology
|
August 30, 2002
The impact of transfusion of leucodepleted platelet concentrates on cytomegalovirus disease after allogeneic stem cell transplantation
Milind D Ronghe, Annabel B M Foot, Jaqueline M Cornish, et al.
American Journal of Medical Genetics. Part A
|
October 10, 2012
The Barth Syndrome Registry: distinguishing disease characteristics and growth data from a longitudinal study
Amy E Roberts, Connie Nixon, Colin G Steward, et al.
Clinical Chemistry
|
December 12, 2007
Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndrome
Willem Kulik, Henk van Lenthe, Femke S Stet, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2015
Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
Ann Bowron, Julie Honeychurch, Maggie Williams, et al.
Journal of Inherited Metabolic Disease
|
August 13, 2014
Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
Ann Bowron, Julie Honeychurch, Maggie Williams, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
December 8, 2009
Very long chain fatty acid levels in patients diagnosed with multiple sclerosis
Alastair Wilkins, Gillian Ingram, Anny Brown, et al.
Case Reports in Radiology
|
January 10, 2015
Lobar Collapse and Obliteration of Air Bronchogram Allowing Early Diagnosis of Endobronchial Aspergillus Infection following Hematopoietic Stem Cell Transplantation
Elizabeth Thompson, Manigandan S Thyagarajan, Elizabeth Johnson, et al.
Pediatric Transplantation
|
August 24, 2012
Successful cord blood transplantation in a patient with malignant infantile osteopetrosis and hemophilia
David Buchbinder, Colin G Steward, Geetha Puthenveetil, et al.
Journal of Inherited Metabolic Disease
|
October 31, 2012
Diagnosis of Barth syndrome using a novel LC-MS/MS method for leukocyte cardiolipin analysis
Ann Bowron, Robert Frost, Vicki E C Powers, et al.
Journal of Pediatric Orthopedics. Part B
|
May 14, 2015
A severe systemic presentation of pigmented villonodular synovitis in a child with underlying Chediak-Higashi syndrome
Victoria L True, Fergal P Monsell, Tanya A Smith, et al.
British Journal of Haematology
|
August 30, 2002
The impact of transfusion of leucodepleted platelet concentrates on cytomegalovirus disease after allogeneic stem cell transplantation
Milind D Ronghe, Annabel B M Foot, Jaqueline M Cornish, et al.
American Journal of Medical Genetics. Part A
|
October 10, 2012
The Barth Syndrome Registry: distinguishing disease characteristics and growth data from a longitudinal study
Amy E Roberts, Connie Nixon, Colin G Steward, et al.
Clinical Chemistry
|
December 12, 2007
Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndrome
Willem Kulik, Henk van Lenthe, Femke S Stet, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2015
Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
Ann Bowron, Julie Honeychurch, Maggie Williams, et al.
Journal of Inherited Metabolic Disease
|
August 13, 2014
Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
Ann Bowron, Julie Honeychurch, Maggie Williams, et al.
Page
of 4