Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Bruni, J. E.
del Bigio, M. R.
Cardoso, E. R.
and
Persaud, T. V. N.
1988.
Neuropathology of congenital hydrocephalus in the SUMS/NP mouse.
Acta Neurochirurgica,
Vol. 92,
Issue. 1-4,
p.
118.
1988.
Focal Cortical Dysplasia.
Journal of Neurosurgery,
Vol. 69,
Issue. 3,
Bruni, J.E.
Del Bigio, M.R.
Cardoso, E.R.
and
Persaud, T.V.N.
1988.
Hereditary hydrocephalus in laboratory animals and humans.
Experimental pathology,
Vol. 35,
Issue. 4,
p.
239.
Friede, Reinhard L.
1989.
Developmental Neuropathology.
p.
231.
Leech, Richard W.
1989.
The Cerebrospinal Fluid.
p.
45.
Bibby, Kim
and
McFadzean, Robert
1991.
Aqueduct stenosis and its effect on vision.
Neuro-Ophthalmology,
Vol. 11,
Issue. 6,
p.
297.
Winter, Robin M.
and
Baraitser, Michael
1991.
Multiple Congenital Anomalies.
p.
1.
Lorenzo, Nicholas Y.
Leibrock, Lyal G.
and
Lorenzo, Agapito S.
1991.
A single case of huntington's disease simultaneously occurring with obstructive hydrocephalus.
Surgical Neurology,
Vol. 35,
Issue. 2,
p.
136.
Schrander‐Stumpel, Constance
Höweler, Chris
Jones, Marilyn
Sommer, Annemarie
Stevens, Cathy
Tinschert, Sigrid
Israel, Jeanette
and
Fryns, Jean Pierre
1995.
Spectrum of X‐linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families.
American Journal of Medical Genetics,
Vol. 57,
Issue. 1,
p.
107.
Kenwrick, S
Jouet, M
and
Donnai, D
1996.
X linked hydrocephalus and MASA syndrome..
Journal of Medical Genetics,
Vol. 33,
Issue. 1,
p.
59.
Oi, Shizuo
Shimoda, Masami
Shibata, Masayoshi
Honda, Yumie
Togo, Kouji
Shinoda, Masaki
Tsugane, Ryuichi
and
Sato, Osamu
2000.
Pathophysiology of long-standing overt ventriculomegaly in adults.
Journal of Neurosurgery,
Vol. 92,
Issue. 6,
p.
933.
Parisi, Melissa A.
Kapur, Raj P.
Neilson, Ian
Hofstra, Robert M.W.
Holloway, Lynda W.
Michaelis, Ron C.
and
Leppig, Kathleen A.
2002.
Hydrocephalus and intestinal aganglionosis: Is L1CAM a modifier gene in Hirschsprung disease?.
American Journal of Medical Genetics,
Vol. 108,
Issue. 1,
p.
51.
Zhang, Jun
Williams, Michael A.
and
Rigamonti, Daniele
2006.
Genetics of human hydrocephalus.
Journal of Neurology,
Vol. 253,
Issue. 10,
p.
1255.
Vogel, P.
Read, R. W.
Hansen, G. M.
Payne, B. J.
Small, D.
Sands, A. T.
and
Zambrowicz, B. P.
2012.
Congenital Hydrocephalus in Genetically Engineered Mice.
Veterinary Pathology,
Vol. 49,
Issue. 1,
p.
166.
Munch, Tina Noergaard
Rostgaard, Klaus
Rasmussen, Marie-Louise Hee
Wohlfahrt, Jan
Juhler, Marianne
and
Melbye, Mads
2012.
Familial aggregation of congenital hydrocephalus in a nationwide cohort.
Brain,
Vol. 135,
Issue. 8,
p.
2409.
Gupta, Deepak
Singla, Raghav
and
Dash, Chinmay
2017.
Hydrocephalus.
p.
35.