Recurrence risks in mental retardation.

Por Crow, Y J, Tolmie, J L
Publicado em 1998

Insulin dependent diabetes in childhood and material deprivation in northern England, 1977-86.

Por Crow, Y J, Alberti, K G, Parkin, J M
Publicado em 1991

Therapies in Aicardi–Goutières syndrome

Por Crow, Y J, Vanderver, A, Orcesi, S, Kuijpers, T W, Rice, G I
Publicado em 2014

Aicardi-Goutières Syndrome: Neuroradiologic Findings and Follow-Up

Por Uggetti, C., La Piana, R., Orcesi, S., Egitto, M.G., Crow, Y.J., Fazzi, E.
Publicado no AJNR Am J Neuroradiol (2009)

A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.

Por Ghaffari, S R, Boyd, E, Tolmie, J L, Crow, Y J, Trainer, A H, Connor, J M
Publicado em 1998

Treatment of Gastrointestinal Bleeding in a Probable Case of Cerebroretinal Microangiopathy with Calcifications and Cysts

Por Briggs, T.A., Hubbard, M., Hawkins, C., Cole, T., Livingston, J.H., Crow, Y.J., Pigott, A.
Publicado em 2011

"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome.

Por Crow, Y J, Zuberi, S M, McWilliam, R, Tolmie, J L, Hollman, A, Pohl, K, Stephenson, J B
Publicado em 1998

Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype

Por Clarke, S. L. N., Robertson, L., Rice, G. I., Seabra, L., Hilliard, T. N., Crow, Y. J., Ramanan, A. V.
Publicado no Pediatr Rheumatol Online J (2020)

Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from Scotland.

Por Munroe, P B, Greene, N D, Leung, K Y, Mole, S E, Gardiner, R M, Mitchison, H M, Stephenson, J B, Crow, Y J
Publicado em 1998

ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters

Por Uettwiller, F, Sarrabay, G, Rodero, M P, Rice, G I, Lagrue, E, Marot, Y, Deiva, K, Touitou, I, Crow, Y J, Quartier, P
Publicado no RMD Open (2016)

Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi–Goutières and Singleton–Merten syndromes

Por Bursztejn, A.-C., Briggs, T.A., del Toro Duany, Y., Anderson, B.H., O’Sullivan, J., Williams, S.G., Bodemer, C., Fraitag, S., Gebhard, F., Leheup, B., Lemelle, I., Oojageer, A., Raffo, E., Schmitt, E., Rice, G.I., Hur, S., Crow, Y.J.
Publicado no Br J Dermatol (2015)

A second locus for Aicardi‐Goutières syndrome at chromosome 13q14–21

Por Ali, M, Highet, L J, Lacombe, D, Goizet, C, King, M D, Tacke, U, van der Knaap, M S, Lagae, L, Rittey, C, Brunner, H G, van Bokhoven, H, Hamel, B, Oade, Y A, Sanchis, A, Desguerre, I, Cau, D, Mathieu, N, Moutard, M L, Lebon, P, Kumar, D, Jackson, A P, Crow, Y J
Publicado em 2006

Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21

Por Crow, Y. J., Jackson, A. P., Roberts, E., van Beusekom, E., Barth, P., Corry, P., Ferrie, C. D., Hamel, B. C. J., Jayatunga, R., Karbani, G., Kálmánchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., Stephenson, J. B. P., Tolmie, J. L., Verrips, A., Voit, T., van Bokhoven, H., Brunner, H. G., Woods, C. G.
Publicado em 2000