Hypothyroidism in the Newborn Period

Por Wassner, Ari J., Brown, Rosalind S.
Publicado em 2013

Congenital hypothyroidism: insights into pathogenesis and treatment

Por Cherella, Christine E., Wassner, Ari J.
Publicado no Int J Pediatr Endocrinol (2017)

Isolated Central Hypothyroidism in Young Siblings as a Manifestation of PROP1 Deficiency: Clinical Impact of Whole Exome Sequencing

Por Wassner, Ari J., Cohen, Laurie E., Hechter, Eliana, Dauber, Andrew
Publicado em 2013

Severe hypercalcemia due to subcutaneous fat necrosis: presentation, management and complications

Por Shumer, Daniel E., Thaker, Vidhu, Taylor, George A., Wassner, Ari J.
Publicado em 2014

Liothyronine Improves Biochemical Control of Congenital Hypothyroidism in Patients with Central Resistance to Thyroid Hormone

Por Paone, Laura, Fleisch, Abby F., Feldman, Henry A., Brown, Rosalind S., Wassner, Ari J.
Publicado no J Pediatr (2016)

Myocardial Induction of Type 3 Deiodinase in Dilated Cardiomyopathy

Por Wassner, Ari J., Jugo, Rebecca H., Dorfman, David M., Padera, Robert F., Maynard, Michelle A., Zavacki, Ann M., Jay, Patrick Y., Huang, Stephen A.
Publicado no Thyroid (2017)

Fourteen Monogenic Genes Account for 15% of Nephrolithiasis/Nephrocalcinosis

Por Halbritter, Jan, Baum, Michelle, Hynes, Ann Marie, Rice, Sarah J., Thwaites, David T., Gucev, Zoran S., Fisher, Brittany, Spaneas, Leslie, Porath, Jonathan D., Braun, Daniela A., Wassner, Ari J., Nelson, Caleb P., Tasic, Velibor, Sayer, John A., Hildebrandt, Friedhelm
Publicado no J Am Soc Nephrol (2015)

Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis

Por Braun, Daniela Anne, Lawson, Jennifer Ashley, Gee, Heon Yung, Halbritter, Jan, Shril, Shirlee, Tan, Weizhen, Stein, Deborah, Wassner, Ari J., Ferguson, Michael A., Gucev, Zoran, Fisher, Brittany, Spaneas, Leslie, Varner, Jennifer, Sayer, John A., Milosevic, Danko, Baum, Michelle, Tasic, Velibor, Hildebrandt, Friedhelm
Publicado no Clin J Am Soc Nephrol (2016)

Mutations in SLC26A1 Cause Nephrolithiasis

Por Gee, Heon Yung, Jun, Ikhyun, Braun, Daniela A., Lawson, Jennifer A., Halbritter, Jan, Shril, Shirlee, Nelson, Caleb P., Tan, Weizhen, Stein, Deborah, Wassner, Ari J., Ferguson, Michael A., Gucev, Zoran, Sayer, John A., Milosevic, Danko, Baum, Michelle, Tasic, Velibor, Lee, Min Goo, Hildebrandt, Friedhelm
Publicado no Am J Hum Genet (2016)

A Standardized Assessment of Thyroid Nodules in Children Confirms Higher Cancer Prevalence Than in Adults

Por Gupta, Anjuli, Ly, Samantha, Castroneves, Luciana A., Frates, Mary C., Benson, Carol B., Feldman, Henry A., Wassner, Ari J., Smith, Jessica R., Marqusee, Ellen, Alexander, Erik K., Barletta, Justine, Doubilet, Peter M., Peters, Hope E., Webb, Susan, Modi, Biren P., Paltiel, Harriet J., Kozakewich, Harry, Cibas, Edmund S., Moore, Francis D., Shamberger, Robert C., Larsen, P. Reed, Huang, Stephen A.
Publicado em 2013

Mice With Hepatocyte-Specific Deficiency of Type 3 Deiodinase Have Intact Liver Regeneration and Accelerated Recovery From Nonthyroidal Illness After Toxin-Induced Hepatonecrosis

Por Castroneves, Luciana A., Jugo, Rebecca H., Maynard, Michelle A., Lee, Jennifer S., Wassner, Ari J., Dorfman, David, Bronson, Roderick T., Ukomadu, Chinweike, Agoston, Agoston T., Ding, Lai, Luongo, Cristina, Guo, Cuicui, Song, Huaidong, Demchev, Valeriy, Lee, Nicholas Y., Feldman, Henry A., Vella, Kristen R., Peake, Roy W., Hartigan, Christina, Kellogg, Mark D., Desai, Anal, Salvatore, Domenico, Dentice, Monica, Huang, Stephen A.
Publicado em 2014

How Are Childhood Thyroid Nodules Discovered: Opportunities for Improving Early Detection

Por Gupta, Anjuli, Ly, Samantha, Castroneves, Luciana A., Frates, Mary C., Benson, Carol B., Feldman, Henry A., Wassner, Ari J., Smith, Jessica R., Marqusee, Ellen, Alexander, Erik K., Barletta, Justine, Muyide, Funmilayo, Doubilet, Peter M., Peters, Hope E., Webb, Susan, Modi, Biren P., Paltiel, Harriet J., Martins, Yolanda, Burmeister, Kelly, Kozakewich, Harry, Hollowell, Monica, Cibas, Edmund S., Moore, Francis D., Shamberger, Robert C., Larsen, P. Reed, Huang, Stephen A.
Publicado em 2013

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

Por Daga, Ankana, Majmundar, Amar J., Braun, Daniela A., Gee, Heon Yung, Lawson, Jennifer A., Shril, Shirlee, Jobst-Schwan, Tilman, Vivante, Asaf, Schapiro, David, Tan, Weizhen, Warejko, Jillian K., Widmeier, Eugen, Nelson, Caleb P., Fathy, Hanan M., Gucev, Zoran, Soliman, Neveen A., Hashmi, Seema, Halbritter, Jan, Halty, Margarita, Kari, Jameela, El-Desoky, Sherif, Ferguson, Michael A., Somers, Michael J.G., Traum, Avram Z., Stein, Deborah R., Daouk, Ghaleb H., Rodig, Nancy M., Katz, Avi, Hanna, Christian, Schwaderer, Andrew L., Sayer, John A., Wassner, Ari J., Mane, Shrikant, Lifton, Richard P., Milosevic, Danko, Tasic, Velibor, Baum, Michelle A., Hildebrandt, Friedhelm
Publicado no Kidney Int (2017)