Thanatophoric dysplasia in identical twins.

le Knisely, A S
Foilsithe 1989

Copper associated childhood cirrhosis.

le Knisely, A S
Foilsithe 1995

Liver Biopsy Interpretation

le KNISELY, A
Foilsithe 2001

Lethal osteogenesis imperfecta.

le Knisely, A S, Abuelo, D, Byers, P H
Foilsithe 1989

Vasotropic light-chain amyloidosis and ischaemic cholangiopathy

le Johnston, Emma L, Wilkinson, Mark, Knisely, A S
Foilsithe in BMJ Case Rep (2015)

Expression in Organ Culture of Agouti Locus Genes of the Mouse

le Knisely, A. S., Gasser, David L., Silvers, Willys K.
Foilsithe 1975

Byler's syndrome

le KNISELY, A, AGOSTINI, R, ZITELLI, B, KOCOSHIS, S, BOYLE, J
Foilsithe 1997

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

le Knisely, A S, Richardson, A, Abuelo, D, Casey, S, Singer, D B
Foilsithe 1988

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

le Hardy, L., Hansen, J. L., Kushner, J. P., Knisely, A. S.
Foilsithe 1990

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

le Knisely, A. S., Harford, J. B., Klausner, R. D., Taylor, S. R.
Foilsithe 1989

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

le Knisely, A.T., Girton, M.R., Hintz, H.C., Modesitt, S.C.
Foilsithe in Gynecol Oncol Rep (2018)

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

le Narchi, Hassib, Alhefeiti, Suhailah, Althabahi, Fatmah, Hertecant, Jozef, Knisely, A. S., Souid, Abdul-Kader
Foilsithe in Saudi J Gastroenterol (2017)

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

le Zhang, Mei-Hong, Knisely, A. S., Wang, Neng-li, Gong, Jing-Yu, Wang, Jian-She
Foilsithe in BMC Gastroenterol (2016)

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

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

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

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

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis

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

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

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

Influence of Donor Criteria on Early Outcome After Intestinal Transplantation

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

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

le 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
Foilsithe 1997

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

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