Torthaí cuardaigh - Sandesh C.S. Nagamani
- 1 - 20 toradh as 42 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Argininosuccinate lyase deficiency de réir Sandesh C.S. Nagamani, Ayelet Erez, Brendan Lee
Foilsithe / Cruthaithe 2012Revisão -
2
Argininosuccinate lyase deficiency—Argininosuccinic aciduria and beyond de réir Ayelet Erez, Sandesh C. Sreenath Nagamani, Brendan Lee
Foilsithe / Cruthaithe 2011Revisão -
3
Arginase I deficiency: Severe infantile presentation with hyperammonemia: More common than reported? de réir Shailly Jain‐Ghai, Sandesh C.S. Nagamani, Susan Blasér, Komudi Siriwardena, Annette Feigenbaum
Foilsithe / Cruthaithe 2011Artigo -
4
Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders de réir Lindsay C. Burrage, Sandesh C.S. Nagamani, Philippe M. Campeau, Brendan H. Lee
Foilsithe / Cruthaithe 2014Revisão -
5
Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders de réir Lindsay C. Burrage, Mahim Jain, Laura Gandolfo, Brendan H. Lee, Sandesh C.S. Nagamani
Foilsithe / Cruthaithe 2014Artigo -
6
Approach to the Patient: Pharmacological Therapies for Fracture Risk Reduction in Adults With Osteogenesis Imperfecta de réir Winnie Liu, Brendan Lee, Sandesh C.S. Nagamani, Lindsey Nicol, Frank Rauch, Eric T. Rush, V. Reid Sutton, Eric Orwoll
Foilsithe / Cruthaithe 2023Revisão -
7
Argininosuccinic aciduria: Recent pathophysiological insights and therapeutic prospects de réir Julien Baruteau, Carmen Dı́ez-Fernández, Shaul Lerner, Giusy Ranucci, Paul Gissen, Carlo Dionisi‐Vici, Sandesh C.S. Nagamani, Ayelet Erez, Johannes Häberle
Foilsithe / Cruthaithe 2019Revisão -
8
Early prediction of phenotypic severity in Citrullinemia Type 1 de réir Matthias Zielonka, Stefan Kölker, Florian Gleich, Nicolas Stützenberger, Sandesh C.S. Nagamani, Andrea Gropman, Georg F. Hoffmann, Sven F. Garbade, Roland Posset
Foilsithe / Cruthaithe 2019Artigo -
9
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders de réir Sandesh C.S. Nagamani, Ayelet Erez, Bruria Ben‐Zeev, Moshe Frydman, Susan Winter, Robert S. Zeller, Dima El‐Khechen, Luis Escobar, Paweł Stankiewicz, Ankita Patel, Sau Wai Cheung
Foilsithe / Cruthaithe 2012Artigo -
10
Evaluation of teriparatide treatment in adults with osteogenesis imperfecta de réir Eric Orwoll, Jay R. Shapiro, Sandra Veith, Ying Wang, Jodi Lapidus, Chaim Vanek, Jan L. Reeder, Tony M. Keaveny, David C. Lee, Mary A. Mullins, Sandesh C.S. Nagamani, Brendan Lee
Foilsithe / Cruthaithe 2014Artigo -
11
Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation de réir Zixue Jin, Jordan Kho, Brian Dawson, Ming‐Ming Jiang, Yuqing Chen, Saima Ali, Lindsay C. Burrage, Monica Grover, Donna Palmer, Dustin L. Turner, Philip Ng, Sandesh C.S. Nagamani, Brendan Lee
Foilsithe / Cruthaithe 2020Artigo -
12
Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency de réir Lindsay C. Burrage, Qin Sun, Sarah H. Elsea, Ming‐Ming Jiang, Sandesh C.S. Nagamani, Arthur E. Frankel, Everett Stone, Susan E. Alters, Dale E. Johnson, Scott W. Rowlinson, George Georgiou, Brendan Lee
Foilsithe / Cruthaithe 2015Artigo -
13
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 de réir Sandesh C. Sreenath Nagamani, Ayelet Erez, Joseph Shen, Chumei Li, Elizabeth Roeder, Sarah K. Cox, Lefkothea Karaviti, Margret Pearson, Sung‐Hae Kang, Trilochan Sahoo, Seema R. Lalani, Paweł Stankiewicz, V. Reid Sutton, Sau Wai Cheung
Foilsithe / Cruthaithe 2009Artigo -
14
Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes de réir Susan A. Berry, Uta Lichter‐Konecki, George A. Díaz, Shawn E. McCandless, William J. Rhead, Wendy E. Smith, Cynthia LeMons, Sandesh C.S. Nagamani, Dion F. Coakley, Masoud Mokhtarani, Bruce F. Scharschmidt, Brendan Lee
Foilsithe / Cruthaithe 2014Artigo -
15
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3 de réir Shen Gu, Bo Yuan, Ian M. Campbell, Christine R. Beck, Claudia M.B. Carvalho, Sandesh C.S. Nagamani, Ayelet Erez, Ankita Patel, Carlos A. Bacino, Chad A. Shaw, Paweł Stankiewicz, Sau Wai Cheung, Weimin Bi, James R. Lupski
Foilsithe / Cruthaithe 2015Artigo -
16
Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis de réir Shiran Rabinovich, Lital N. Adler, Keren Yizhak, Alona Sarver, Alon Silberman, Shani Agron, Noa Stettner, Qin Sun, Alexander Brandis, Daniel Helbling, Stanley H. Korman, Shalev Itzkovitz, David Dimmock, Igor Ulitsky, Sandesh C.S. Nagamani, Eytan Ruppin, Ayelet Erez
Foilsithe / Cruthaithe 2015Artigo -
17
Untargeted metabolomic profiling reveals multiple pathway perturbations and new clinical biomarkers in urea cycle disorders de réir Lindsay C. Burrage, Lillian R Thistlethwaite, Bridget M. Stroup, Qin Sun, Marcus J. Miller, Sandesh C.S. Nagamani, William Craigen, Fernando Scaglia, V. Reid Sutton, Brett H. Graham, Adam D. Kennedy, Aleksandar Milosavljević, Brendan Lee, Sarah H. Elsea
Foilsithe / Cruthaithe 2019Artigo -
18
Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an <i>IFITM</i> <i>5</i> Mutation de réir Jay R. Shapiro, Caressa Lietman, Monica Grover, James T. Lu, Sandesh C.S. Nagamani, Brian C. Dawson, Dustin Baldridge, Matthew N. Bainbridge, D.H. Cohn, Maria Blazo, Timothy T. Roberts, Feng-Shu Brennen, Yimei Wu, Richard A. Gibbs, Pamela Melvin, Philippe M. Campeau, Brendan Lee
Foilsithe / Cruthaithe 2013Artigo -
19
Next-generation sequencing for disorders of low and high bone mineral density de réir Gautam Sule, Philippe M. Campeau, V. W. Zhang, Sandesh C.S. Nagamani, Brian C. Dawson, Monica Grover, Carlos A. Bacino, V. Reid Sutton, Nicola Brunetti‐Pierri, James T. Lu, Edmond G. Lemire, Richard A. Gibbs, Daniel H. Cohn, Hong Cui, L. Wong, Brendan H. Lee
Foilsithe / Cruthaithe 2013Artigo -
20
A cross‐sectional multicenter study of osteogenesis imperfecta in North America – results from the linked clinical research centers de réir Ruchita Patel, Sandesh C.S. Nagamani, David Cuthbertson, Philippe M. Campeau, J. Krischer, Jay R. Shapiro, Robert D. Steiner, Peter A. Smith, Michael B. Bober, Peter H. Byers, Melanie Pepin, Michaela Durigova, Francis H. Glorieux, Frank Rauch, B.H. Lee, Tracy Hart, V. Reid Sutton
Foilsithe / Cruthaithe 2014Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Medicine
Internal medicine
Gene
Genetics
Biochemistry
Amino acid
Arginine
Chemistry
Urea cycle
Endocrinology
Pathology
Phenotype
Osteogenesis imperfecta
Arginase
Argininosuccinate synthase
Chromosome
Comparative genomic hybridization
Genome
Pediatrics
Argininosuccinate lyase
Copy-number variation
Gene duplication
Hyperammonemia
Bone mineral
Cell biology
Cohort
Disease
Osteoporosis
Psychiatry