Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference

Meral Gunay-Aygun; Ellis D. Avner; Robert L. Bacallao; Peter L. Choyke; Joseph T. Flynn; Gregory G. Germino; Lisa Guay-Woodford; Peter Harris; Theo Heller; Julie Ingelfinger; Frederick Kaskel; Robert Kleta; Nicholas F. LaRusso; Parvathi Mohan; Gregory J. Pazour; Benjamin L. Shneider; Vicente E. Torres; Patricia Wilson; Colleen Zak; Jing Zhou; William A. Gahl

doi:10.1016/j.jpeds.2006.03.014

Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference

Meral Gunay-Aygun
, Ellis D. Avner
, Robert L. Bacallao
, Peter L. Choyke
, Joseph T. Flynn
, Gregory G. Germino
, Lisa Guay-Woodford
, Peter Harris
, Theo Heller
, Julie Ingelfinger
, Frederick Kaskel
, Robert Kleta
, Nicholas F. LaRusso
, Parvathi Mohan
, Gregory J. Pazour
, Benjamin L. Shneider
, Vicente E. Torres
, Patricia Wilson
, Colleen Zak
, Jing Zhou

William A. Gahl

Research output: Contribution to journal › Article › peer-review

87 Scopus citations

Original language	English
Pages (from-to)	159-164
Number of pages	6
Journal	Journal of Pediatrics
Volume	149
Issue number	2
DOIs	https://doi.org/10.1016/j.jpeds.2006.03.014
State	Published - Aug 2006
Externally published	Yes

Access to Document

10.1016/j.jpeds.2006.03.014

Cite this

Gunay-Aygun, M., Avner, E. D., Bacallao, R. L., Choyke, P. L., Flynn, J. T., Germino, G. G., Guay-Woodford, L., Harris, P., Heller, T., Ingelfinger, J., Kaskel, F., Kleta, R., LaRusso, N. F., Mohan, P., Pazour, G. J., Shneider, B. L., Torres, V. E., Wilson, P., Zak, C., ... Gahl, W. A. (2006). Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference. Journal of Pediatrics, 149(2), 159-164. https://doi.org/10.1016/j.jpeds.2006.03.014

@article{9a1e40c619bc4ba391f9279f0e21aa9f,

title = "Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference",

author = "Meral Gunay-Aygun and Avner, \{Ellis D.\} and Bacallao, \{Robert L.\} and Choyke, \{Peter L.\} and Flynn, \{Joseph T.\} and Germino, \{Gregory G.\} and Lisa Guay-Woodford and Peter Harris and Theo Heller and Julie Ingelfinger and Frederick Kaskel and Robert Kleta and LaRusso, \{Nicholas F.\} and Parvathi Mohan and Pazour, \{Gregory J.\} and Shneider, \{Benjamin L.\} and Torres, \{Vicente E.\} and Patricia Wilson and Colleen Zak and Jing Zhou and Gahl, \{William A.\}",

note = "Funding Information: Supported in part by the Intramural Research Program of the NIH, specifically, that of the National Human Genome Research Institute, and by the Office of Rare Diseases, Office of the Director, NIH, and ARPKD/CHF Alliance. Funding Information: Researchers and clinicians with expertise in autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) and related fields met on May 5-6, 2005, on the National Institutes of Health (NIH) campus for a 1.5-day symposium sponsored by the NIH Office of Rare Diseases, the National Human Genome Research Institute (NHGRI), and in part by the ARPKD/CHF Alliance. The meeting addressed the present status and the future of ARPKD/CHF research. ",

year = "2006",

month = aug,

doi = "10.1016/j.jpeds.2006.03.014",

language = "English",

volume = "149",

pages = "159--164",

journal = "Journal of Pediatrics",

issn = "0022-3476",

publisher = "Elsevier Inc.",

number = "2",

}

Gunay-Aygun, M, Avner, ED, Bacallao, RL, Choyke, PL, Flynn, JT, Germino, GG, Guay-Woodford, L, Harris, P, Heller, T, Ingelfinger, J, Kaskel, F, Kleta, R, LaRusso, NF, Mohan, P, Pazour, GJ, Shneider, BL, Torres, VE, Wilson, P, Zak, C, Zhou, J & Gahl, WA 2006, 'Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference', Journal of Pediatrics, vol. 149, no. 2, pp. 159-164. https://doi.org/10.1016/j.jpeds.2006.03.014

Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference. / Gunay-Aygun, Meral; Avner, Ellis D.; Bacallao, Robert L. et al.
In: Journal of Pediatrics, Vol. 149, No. 2, 08.2006, p. 159-164.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis

T2 - Summary statement of a First National Institutes of Health/Office of Rare Diseases conference

AU - Gunay-Aygun, Meral

AU - Avner, Ellis D.

AU - Bacallao, Robert L.

AU - Choyke, Peter L.

AU - Flynn, Joseph T.

AU - Germino, Gregory G.

AU - Guay-Woodford, Lisa

AU - Harris, Peter

AU - Heller, Theo

AU - Ingelfinger, Julie

AU - Kaskel, Frederick

AU - Kleta, Robert

AU - LaRusso, Nicholas F.

AU - Mohan, Parvathi

AU - Pazour, Gregory J.

AU - Shneider, Benjamin L.

AU - Torres, Vicente E.

AU - Wilson, Patricia

AU - Zak, Colleen

AU - Zhou, Jing

AU - Gahl, William A.

N1 - Funding Information: Supported in part by the Intramural Research Program of the NIH, specifically, that of the National Human Genome Research Institute, and by the Office of Rare Diseases, Office of the Director, NIH, and ARPKD/CHF Alliance. Funding Information: Researchers and clinicians with expertise in autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) and related fields met on May 5-6, 2005, on the National Institutes of Health (NIH) campus for a 1.5-day symposium sponsored by the NIH Office of Rare Diseases, the National Human Genome Research Institute (NHGRI), and in part by the ARPKD/CHF Alliance. The meeting addressed the present status and the future of ARPKD/CHF research.

PY - 2006/8

Y1 - 2006/8

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U2 - 10.1016/j.jpeds.2006.03.014

DO - 10.1016/j.jpeds.2006.03.014

M3 - Article

C2 - 16887426

AN - SCOPUS:33746655404

SN - 0022-3476

VL - 149

SP - 159

EP - 164

JO - Journal of Pediatrics

JF - Journal of Pediatrics

IS - 2

ER -