Microbial genomics: from sequence to function.

por Schwartz, I
Publicado 2000

Prevalence of tick-borne pathogens in Ixodes scapularis in a rural New Jersey County.

por Varde, S, Beckley, J, Schwartz, I
Publicado 1998

Deer ticks (Ixodes scapularis) and the agents of Lyme disease and human granulocytic ehrlichiosis in a New York City park.

por Daniels, T J, Falco, R C, Schwartz, I, Varde, S, Robbins, R G
Publicado 1997

Infant mortality in Brazil attributable to inborn errors of metabolism associated with sudden death: a time-series study (2002–2014)

por de Bitencourt, F. H., Schwartz, I. V. D., Vianna, F. S. L.
Publicado 2019

THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY

por Brecher, G., Laqueur, G. L., Cronkite, E. P., Edelman, P. M., Schwartz, I. L.
Publicado 1965

Combined Transplantation of Human Neuronal and Mesenchymal Stem Cells following Spinal Cord Injury

por Park, D. Y., Mayle, R. E., Smith, R. L., Corcoran-Schwartz, I., Kharazi, A. I., Cheng, I.
Publicado 2013

Quality of life in mucopolysaccharidoses: construction of a specific measure using the focus group technique

por Oliveira, M. R., Schwartz, I., Costa, L. S., Maia, H., Ribeiro, M., Guerreiro, L. B., Acosta, A., Rocha, N. S.
Publicado 2018

Quality of life and adherence to treatment in early-treated Brazilian phenylketonuria pediatric patients

por Vieira, E., Maia, H.S., Monteiro, C.B., Carvalho, L.M., Tonon, T., Vanz, A.P., Schwartz, I.V.D., Ribeiro, M.G.
Publicado 2017

Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis

por Belmont, John W, Reid, Barbara, Taylor, William, Baker, Susan S, Moore, Warren H, Morriss, Michael C, Podrebarac, Susan M, Glass, Nancy, Schwartz, I David
Publicado 2002

Burden of phenylketonuria in Latin American patients: a systematic review and meta-analysis of observational studies

por Pessoa, A. L. S., Martins, A. M., Ribeiro, E. M., Specola, N., Chiesa, A., Vilela, D., Jurecki, E., Mesojedovas, D., Schwartz, I. V. D.
Publicado 2022

Severity score system for progressive myelopathy: development and validation of a new clinical scale

por Castilhos, R.M., Blank, D., Netto, C.B.O., Souza, C.F.M., Fernandes, L.N.T., Schwartz, I.V.D., Giugliani, R., Jardim, L.B.
Publicado 2012

Exome sequencing for mucolipidosis III: Detection of a novel GNPTAB gene mutation in a patient with a very mild phenotype

por Sperb-Ludwig, F., Alegra, T., Velho, R.V., Ludwig, N., Kim, C.A., Kok, F., Kitajima, J.P., van Meel, E., Kornfeld, S., Burin, M.G., Schwartz, I.V.D.
Publicado 2014

Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation

por Klammt, Jürgen, Neumann, David, Gevers, Evelien F., Andrew, Shayne F., Schwartz, I. David, Rockstroh, Denise, Colombo, Roberto, Sanchez, Marco A., Vokurkova, Doris, Kowalczyk, Julia, Metherell, Louise A., Rosenfeld, Ron G., Pfäffle, Roland, Dattani, Mehul T., Dauber, Andrew, Hwa, Vivian
Publicado 2018

Successful domino liver transplantation in maple syrup urine disease using a related living donor

por Feier, F.H., Miura, I.K., Fonseca, E.A., Porta, G., Pugliese, R., Porta, A., Schwartz, I.V.D., Margutti, A.V.B., Camelo, J.S., Yamaguchi, S.N., Taveira, A.T., Candido, H., Benavides, M., Danesi, V., Guimaraes, T., Kondo, M., Chapchap, P., Seda, J.
Publicado 2014

Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme(®)) therapy

por Braunlin, E., Rosenfeld, H., Kampmann, C., Johnson, J., Beck, M., Giugliani, R., Guffon, N., Ketteridge, D., Sá Miranda, C. M., Scarpa, M., Schwartz, I. V., Leão Teles, E., Wraith, J. E., Barrios, P., Dias da Silva, E., Kurio, G., Richardson, M., Gildengorin, G., Hopwood, J. J., Imperiale, M., Schatz, A., Decker, C., Harmatz, P.
Publicado 2012