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by S M Huson , D A S Compstont , P S Harper
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Citations
31
Von Recklinghausen neurofibromatosis: clinical and population study in South East Wales.
- SM, PS, et al. - 1988
26
Von Recklinghausen neurofibromatosis
- VM
11
Das Gupta TK: Von Recklinghausen’s disease: a clinicopathological study. Ann Surg 175:86–104,
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10
A clinical, pathological, and genetic study of multiple neurofibromatosis. Charles C. Thomas,
- FW, WJ, et al. - 1956
8
Multipoint linkage analysis in neurofibromatosis type 1: An international collaboration
- Goldgar, Green, et al. - 1989
8
Clinical and genetic investigations into tuberous sclerosis and Recklinghausen's neurofibromatosis. Acta psychiat. scand., Suppl
- Borberg - 1951
6
BD: Penetrance and variability in neurofibromatosis: A genetic study of 60 families
- JC, JM, et al. - 1979
3
Eichner JE: Neurofibromatosis: Phenotype, Natural History and Pathogenesis
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3
Kinnier-Wilson LM, Sti ller CA. Gl iomas in neurofibromatosis: a series of 89 cases with evidence of enhanced malignancy in associated cerebellar astrocytomas. Pathol Annu 1985;20:331
- EB
3
Von Recklinghausen neurofibromatosis. II. Incidence of optic glomata. Ophthalmology
- RA, LP, et al.
2
fitness, mutation rate, and effect of parental transmission on severity
- Prevalence - 1989
1
et al. Gcne for von Rccklinghauscn ncurofibromatosis is in the pcricentromcric region of chromosome 17
- K
1
Roulcau GA. Ozclius LG. et al. Genetic linkage of von Recklinghauscn ncurofibromatosis to the ncrvc growth factor rcceptor genc. Cell
- BR
1
Neurofibromatosis (von Recklinghausen's disease): a clinical-psychiatric and genetic study
- 7Samuelsson - 1981
1
Linkage analysis of pcripheral neurofibromatosis (von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy
- SM, AL, et al.
1
Ophthalmic manifestations of von Recklinghausen neurofibromatosis
- SM, Jones, et al.
1
Brief clinical report. Aqueductal stenosis leading to hydrocephalus-an unusual manifestation of neurofibromatosis
- Horwich, VM, et al.
1
Farndon JR, Shepherd A, et al. Phaeochromocytoma in 72 patients: clinical and diagnostic features, treatment and 6 long term results
- IM
1
Duodenal carcinoid, phaeochromocytoma and neurofibromatosis: islet cell tumor, phaeochromocytoma and the von Hippel Lindau complex: two distinctive neuroendocrine syndromes
- DFR, GT, et al.
1
9 Morrissy RT, Riseborough EJ, Hall JE. Congenital pseudoarthrosis of the tibia
- AL, JM, et al.
1
Neurofibromatosis scoliosis. Natural history and results of treatment in thirty-seven cases. J Bone Joint Surg (Am
- JH, EJ, et al.
1
Cafe-au-lait spots in school children. Arch Dis Child
- RG, NJ, et al.
1
Rigel DS, Friedman RJ. Levenstein M. Prevalence of congenital nevus-like-nevi. r,^vi spilli, and cafe au lait spots. Arch Dermatol
- AW, LJ
1
Iris hamartomata as diagnostic criterion in neurofibromatosis. Neuropediatrics
- E
1
NIH consensus development statement. 33 Treves F. A case of congenital deformity
- Neurofibromatosis
1
Luxenburg MN. Pulsating enophthalmos and choroidal hamartomas: two rare stigmata of neurofibromatosis
- PJ, JS
1
Cerebrovascular Correspondence to Dr S M Huson, Department of changes in neurofibromatosis
- SM