Torthaí cuardaigh - Robert D. Steiner
- 1 - 20 toradh as 44 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Osteogenesis imperfecta: Recent findings shed new light on this once well-understood condition de réir Donald Basel, Robert D. Steiner
Foilsithe / Cruthaithe 2009Revisão -
2
Epidemiology, diagnosis, and treatment of cerebrotendinous xanthomatosis (CTX) de réir Gerald Salen, Robert D. Steiner
Foilsithe / Cruthaithe 2017Revisão -
3
Allelic prevalence and geographic distribution of cerebrotendinous xanthomatosis de réir Tiziano Pramparo, Robert D. Steiner, Steve Rodems, Celia Jenkinson
Foilsithe / Cruthaithe 2023Artigo -
4
Bisphosphonate therapy for osteogenesis imperfecta de réir Kerry Dwan, Carrie A. Phillipi, Robert D. Steiner, Donald Basel
Foilsithe / Cruthaithe 2016Revisão -
5
Treatment of Smith–Lemli–Opitz syndrome and other sterol disorders de réir Melissa Svoboda, Jill M. Christie, Yasemen Eroğlu, Kurt A. Freeman, Robert D. Steiner
Foilsithe / Cruthaithe 2012Revisão -
6
Smith–Lemli–Opitz syndrome de réir Andrea E. DeBarber, Yasemen Eroğlu, Louise S. Merkens, Anuradha S. Pappu, Robert D. Steiner
Foilsithe / Cruthaithe 2011Revisão -
7
Correlates of language impairment in children with galactosaemia de réir Nancy L. Potter, Jordan Lazarus, Joyce M. Johnson, Robert D. Steiner, Lawrence D. Shriberg
Foilsithe / Cruthaithe 2008Artigo -
8
Variability in phenylalanine control predicts IQ and executive abilities in children with phenylketonuria de réir Anna Hood, Dorothy K. Grange, Shawn E. Christ, Robert D. Steiner, Desirée A. White
Foilsithe / Cruthaithe 2014Artigo -
9
Smith-Lemli-Opitz Syndrome: Clinical, Biochemical, and Genetic Insights With Emerging Treatment Opportunities de réir Amy Kritzer, Rana Dutta, Tiziano Pramparo, Jolan Terner-Rosenthal, Pamela Vig, Robert D. Steiner
Foilsithe / Cruthaithe 2025Revisão -
10
Sibling Recurrence Risk and Cross-aggregation of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder de réir Meghan Miller, Erica D. Musser, Gregory S. Young, Brent F. Olson, Robert D. Steiner, Joel T. Nigg
Foilsithe / Cruthaithe 2018Artigo -
11
Evaluation of miglustat as maintenance therapy after enzyme therapy in adults with stable type 1 Gaucher disease: a prospective, open-label non-inferiority study de réir Timothy M. Cox, Dominick Amato, Carla E. M. Hollak, Cecile Paquet Luzy, Mariabeth Silkey, R. Giorgino, Robert D. Steiner
Foilsithe / Cruthaithe 2012Artigo -
12
Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal Defects de réir Susan W. Robinson, Cynthia D. Morris, Elizabeth Goldmuntz, Mark D. Reller, Melanie A. Jones, Robert D. Steiner, Cheryl L. Maslen
Foilsithe / Cruthaithe 2003Artigo -
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A useful multi-analyte blood test for cerebrotendinous xanthomatosis de réir Andrea E. DeBarber, Jenny Luo, Roberto Giugliani, Carolina Fischinger Moura de Souza, John Chiang, Louise S. Merkens, Anuradha S. Pappu, Robert D. Steiner
Foilsithe / Cruthaithe 2014Artigo -
16
Shared familial transmission of autism spectrum and attention‐deficit/hyperactivity disorders de réir Erica D. Musser, Elizabeth Hawkey, Svetlana S. Kachan‐Liu, Paul Lees, Jean‐Baptiste Roullet, Katrina A.B. Goddard, Robert D. Steiner, Joel T. Nigg
Foilsithe / Cruthaithe 2014Artigo -
17
Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications de réir W Feero, Robert D. Steiner, Anne Slavotinek, Tiago Faial, Michael J. Bamshad, Jehannine Austin, Bruce R. Korf, Annette Flanagin, Kirsten Bibbins‐Domingo
Foilsithe / Cruthaithe 2024Editorial -
18
Apolipoprotein E–low density lipoprotein receptor interaction affects spatial memory retention and brain ApoE levels in an isoform-dependent manner de réir Lance A. Johnson, Reid H. J. Olsen, Louise S. Merkens, Andrea E. DeBarber, Robert D. Steiner, Patrick M. Sullivan, Nobuyo Maeda, Jacob Raber
Foilsithe / Cruthaithe 2014Artigo -
19
Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz Syndrome de réir Christopher A. Wassif, Cheryl L. Maslen, Stivelia Kachilele-Linjewile, Don S. Lin, Leesa M. Linck, William E. Connor, Robert D. Steiner, Forbes D. Porter
Foilsithe / Cruthaithe 1998Artigo -
20
Agalsidase Alfa and Kidney Dysfunction in Fabry Disease de réir Michael L. West, Kathy Nicholls, Atul Mehta, Joe T.R. Clarke, Robert D. Steiner, Michael Beck, Bruce A. Barshop, William J. Rhead, Robert Mensah, Markus Ries, Raphael Schiffmann
Foilsithe / Cruthaithe 2009Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Internal medicine
Genetics
Gene
Biochemistry
Pediatrics
Pathology
Cholesterol
Osteogenesis imperfecta
Chemistry
Disease
Enzyme
Enzyme replacement therapy
Psychology
Bioinformatics
Endocrinology
Psychiatry
Reductase
7-Dehydrocholesterol reductase
Cerebrotendinous Xanthomatosis
Phenotype
Smith–Lemli–Opitz syndrome
Sterol
Surgery
Amino acid
Cohort
Developmental psychology
Family medicine
Gastroenterology