Thanatophoric dysplasia in identical twins.

Autor Knisely, A S
Vydáno 1989

Copper associated childhood cirrhosis.

Autor Knisely, A S
Vydáno 1995

Liver Biopsy Interpretation

Autor KNISELY, A
Vydáno 2001

Lethal osteogenesis imperfecta.

Autor Knisely, A S, Abuelo, D, Byers, P H
Vydáno 1989

Vasotropic light-chain amyloidosis and ischaemic cholangiopathy

Autor Johnston, Emma L, Wilkinson, Mark, Knisely, A S
Vydáno v BMJ Case Rep (2015)

Expression in Organ Culture of Agouti Locus Genes of the Mouse

Autor Knisely, A. S., Gasser, David L., Silvers, Willys K.
Vydáno 1975

Byler's syndrome

Autor KNISELY, A, AGOSTINI, R, ZITELLI, B, KOCOSHIS, S, BOYLE, J
Vydáno 1997

Lethal osteogenesis imperfecta associated with 46,XY,inv(7)(p13q22) karyotype.

Autor Knisely, A S, Richardson, A, Abuelo, D, Casey, S, Singer, D B
Vydáno 1988

Neonatal hemochromatosis. Genetic analysis of transferrin-receptor, H-apoferritin, and L-apoferritin loci and of the human leukocyte antigen class I region.

Autor Hardy, L., Hansen, J. L., Kushner, J. P., Knisely, A. S.
Vydáno 1990

Neonatal hemochromatosis. The regulation of transferrin-receptor and ferritin synthesis by iron in cultured fibroblastic-line cells.

Autor Knisely, A. S., Harford, J. B., Klausner, R. D., Taylor, S. R.
Vydáno 1989

Vaginal sarcoidosis without other organ involvement in a patient with a history of endometrial cancer: A case report

Autor Knisely, A.T., Girton, M.R., Hintz, H.C., Modesitt, S.C.
Vydáno v Gynecol Oncol Rep (2018)

Intrahepatic cholestasis in two Omani siblings associated with a novel homozygous ATP8B1 mutation, c.379C>G (p.L127V)

Autor Narchi, Hassib, Alhefeiti, Suhailah, Althabahi, Fatmah, Hertecant, Jozef, Knisely, A. S., Souid, Abdul-Kader
Vydáno v Saudi J Gastroenterol (2017)

Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid

Autor Zhang, Mei-Hong, Knisely, A. S., Wang, Neng-li, Gong, Jing-Yu, Wang, Jian-She
Vydáno v BMC Gastroenterol (2016)

Recurrent acute liver failure associated with novel SCYL1 mutation: A case report

Autor Li, Jia-Qi, Gong, Jing-Yu, Knisely, A S, Zhang, Mei-Hong, Wang, Jian-She
Vydáno v World J Clin Cases (2019)

Co-existence of ABCB11 and DCDC2 disease: Infantile cholestasis requires both next-generation sequencing and clinical-histopathologic correlation

Autor Vogel, Georg-Friedrich, Maurer, Elisabeth, Entenmann, Andreas, Straub, Simon, Knisely, A. S., Janecke, Andreas R., Müller, Thomas
Vydáno v Eur J Hum Genet (2020)

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis

Autor Smyk, Daniel S., Mytilinaiou, Maria G., Grammatikopoulos, Tassos, Knisely, A. S., Mieli-Vergani, Giorgina, Bogdanos, Dimitrios P., Vergani, Diego
Vydáno 2013

Polymorphisms in ABCB11 and ATP8B1 Associated with Development of Severe Intrahepatic Cholestasis in Hodgkin's Lymphoma

Autor Blackmore, Laura, Knisely, A.S., Hartley, Jane L., McKay, Kirsten, Gissen, Paul, Marcus, Robert, Shawcross, Debbie L.
Vydáno 2013

Influence of Donor Criteria on Early Outcome After Intestinal Transplantation

Autor Furukawa, H., Smith, C., Lee, R., Knisely, A.S., Irish, W., Reyes, J., Abu-Elmagd, K., Starzl, T.E., Todo, S.
Vydáno 1997

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24.

Autor Strautnieks, S S, Kagalwalla, A F, Tanner, M S, Knisely, A S, Bull, L, Freimer, N, Kocoshis, S A, Gardiner, R M, Thompson, R J
Vydáno 1997

An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy

Autor Dixon, Peter H., Sambrotta, Melissa, Chambers, Jennifer, Taylor-Harris, Pamela, Syngelaki, Argyro, Nicolaides, Kypros, Knisely, A. S., Thompson, Richard J., Williamson, Catherine
Vydáno v Sci Rep (2017)