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2015, Sixth edition., Lippincott's illustrated reviews, ISBN 1451191774, xi, 664 pages
Book
Neuromuscular Disorders, ISSN 0960-8966, 12/2012, Volume 22, Issue 12, pp. 1105 - 1106
Journal Article
2017, Sixth edition., ISBN 0323371019, xxvi, 1403 pages
Since 1975, Dr. Kenneth Swaiman's classic text has been the reference of choice for authoritative guidance in pediatric neurology, and the 6th Edition... 
Infant | Child | Pediatric neurology | Nervous System Diseases
Book
2009, 4th ed. ; International ed., Lippincott's illustrated reviews, ISBN 160547200X, xii, 564
Book
The New England Journal of Medicine, ISSN 0028-4793, 02/2018, Volume 378, Issue 5, pp. 487 - 488
To the Editor: In two reports regarding patients with type 1 spinal muscular atrophy (Nov. 2 issue), 1,2 researchers describe therapies involving antisense... 
MEDICINE, GENERAL & INTERNAL | Muscular Atrophy, Spinal | Spinal Muscular Atrophies of Childhood | Humans | Index Medicus | Abridged Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2018, Volume 13, Issue 6, pp. e0199657 - e0199657
Journal Article
by Kobayashi, Dione T and Shi, Jing and Stephen, Laurie and Ballard, Karri L and Dewey, Ruth and Mapes, James and Chung, Brett and McCarthy, Kathleen and Swoboda, Kathryn J and Crawford, Thomas O and Li, Rebecca and Plasterer, Thomas and Joyce, Cynthia and Acsadi, G and Campbell, C and Coates, A and Connolly, A.M and Iannaccone, S.T and Khongkhatithum, C and Kissel, J.T and Kolb, S.J and Kunz, N.L and Makris, C and Mathews, K.D and Matthews, D and Schroth, M.K and Vajsar, J and Wang, C.H and Wong, B.L and Sahin, M and Antiel, L and Florence, J and Gee, R and Glanzman, A.M and Hartman, J and King, W and Krosschell, K and Laubenthal, K and McGuire, M and Montes, J and Nelson, L and Owen, J and Patterson, K and Quigley, J and Roman, C and Riley, S and Scholtes, C and Sedlacek, P and Siener, C and Strumpf, S and Wood, J and Ameli, J and Andersen, M and Bell, M and Benton, M and Binner, H and Butler, H and Chelnick, S and Clayton, J and Faut, S and Forrest, S and MacMillan, L and Martensen, M and Montgomery, M and Morehart, P and Pharo, L and Reeves, G and Stephan, C and Taranik, R and Tsai, O and Wedell, V and Wulf, C and Chung, Wendy K and Kaufmann, Petra and Darras, Basil T and Finkel, Richard S and Sproule, Douglas M and Martens, William B and McDermott, Michael P and De Vivo, Darryl C and Constantinescu, A and Foley, A.R and Gooch, CL and Kang, P.B and O'Hagen, J and Oskoui, M and Punyanitya, M and Tawil, R and Yang, M and Dunaway, S and Flinckinger, J and Glanzman, A.M and Montes, J and Quigley, J and Riley, S and Ryan, P.A and Battista, V and Benton, M and Butler, H and Koo, B and ... and Pediat Neuromuscular Clinical Res and Biomarkers Spinal Muscular Atrophy and Biomarkers for Spinal Muscular Atrophy Study Group and Pediatric Neuromuscular Clinical Research Network and the Pediatric Neuromuscular Clinical Research Network and the Biomarkers for Spinal Muscular Atrophy Study Group
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, pp. e60113 - e60113
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, pp. e33572 - e33572
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2004, Volume 351, Issue 3, pp. 302 - 303
To the Editor: With the recent decision of the Food and Drug Administration to ban the sale of ephedra in the United States, a broad discussion of the uses,... 
MEDICINE, GENERAL & INTERNAL | Pregnancy | Phytotherapy - adverse effects | Cocaine - blood | Stroke - chemically induced | Vasoconstrictor Agents - adverse effects | Humans | Caulophyllum - adverse effects | Adult | Female | Plant Preparations - adverse effects | Cocaine - analogs & derivatives | Infant, Newborn
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, pp. e35462 - e35462
Background: Spinal Muscular Atrophy (SMA) is a neurodegenerative motor neuron disorder resulting from a homozygous mutation of the survival of motor neuron 1... 
PLASMA | GENE | SMN | DISEASE | BIOLOGY | PHENYLBUTYRATE | FUNCTIONAL MOTOR SCALE | AMYOTROPHIC-LATERAL-SCLEROSIS | IDENTIFICATION | EXPRESSION | PREDICTION | Severity of Illness Index | Gene Dosage - genetics | Motor Activity - physiology | Biomarkers - urine | Gas Chromatography-Mass Spectrometry | Cross-Sectional Studies | Humans | Child, Preschool | Gene Expression Profiling - methods | Biomarkers - blood | Metabolomics - methods | Case-Control Studies | Amino Acids - metabolism | Fatty Acids, Nonesterified - metabolism | Muscular Atrophy, Spinal - genetics | Tandem Mass Spectrometry | Phenotype | Pilot Projects | Analysis of Variance | Survival of Motor Neuron 2 Protein - genetics | Chromatography, Liquid | Proteomics - methods | Child | RNA | Neurons | Genes | Clinical trials | Amino acids | Development and progression | Fatty acids | Metabolites | Physiological aspects | Genetic aspects | Biological markers | Health aspects | Atrophy, Muscular | Blood proteins | Pediatrics | Neurosciences | Target recognition | Transcription | Copy number | SMN protein | Lung cancer | Neurobiology | Lipids | Identification | Biosynthesis | Kinases | Tissues | Muscular dystrophy | Spinal muscular atrophy | Proteins | Atrophy | Design | Plasma proteins | Rodents | Bioindicators | Children | Lipid metabolism | Cross sections | Urine | Departments | Sensitivity analysis | Cell survival | RNA biosynthesis | Protein biosynthesis | Ribonucleic acid--RNA | Medicine | Neurology | Hypotheses | Fractures | Correlation analysis | Biomarkers | Apoptosis | Index Medicus | Ribonucleic acid
Journal Article