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Subcutaneous neurofibromas
The presence of Neurofibromas in the subcutis. [HPO:sdoelken]
National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
SD-OCT in NIR modality to diagnose retinal microvascular abnormalities in neurofibromatosis type 1
A. Moramarco
,
S. Giustini
,
E. Miraglia
,
M. Sacchetti
Graefe's Archive for Clinical and Experimental…
2018
Corpus ID: 44169580
Dear Editor, Neurofibromatosis type I (NF1), also known as Von Recklinghausen’s disease, is one of the most common autosomal…
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2017
2017
A Novel Frameshift Mutation in Neurofibromin 1 Gene in a Chinese Family with Neurofibromatosis Type 1
Ying-ying Dong
,
Yan-Hong Zhang
,
+7 authors
Yunhua Deng
Chinese Medical Journal
2017
Corpus ID: 3542327
To the Editor: Neurofibromatosis type 1 (NF1) is a common autosomal dominant genetic neurocutaneous disorder mainly characterized…
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2010
2010
Astrocytic Hamartoma of the optic disc and multiple café-au-lait macules in a child with neurofibromatosis type 2
R. Sachdeva
,
D. Rothner
,
E. Traboulsi
,
Brandy C. Hayden
,
P. Rychwalski
Ophthalmic Genetics
2010
Corpus ID: 25013956
Neurofibromatosis type 2 (NF2) is a heritable syndrome characterized by multifocal proliferation of neural crest-derived cells…
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2008
2008
Plexiforme neurofibroma with compromising of the penile function.
R. Barros
,
A. Cavalcanti
,
L. Favorito
Urology
2008
Corpus ID: 7678902
1997
1997
Hair Whorl as an Indicator of a Mediastinal Plexiform Neurofibroma
E. Pivnick
,
T. Lobe
,
S. J. Fitch
,
V. Riccardi
Pediatric dermatology
1997
Corpus ID: 23366107
Abstract: We report a boy with neurofibromatosis type 1 (NF‐1) who had nonspecific respiratoi symptoms and a mediastinal mass. In…
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1997
1997
Neurofibromatosis type 2 (bilateral acoustic schwannomas) demonstrated by Tc-99m (V) DMSA SPECT.
T. Hirano
,
H. Otake
,
T. Shibasaki
,
M. Tamura
Clinical Nuclear Medicine
1997
Corpus ID: 44605270
Tc-99m (V) DMSA clearly demonstrated several cranial meningiomas, bilateral acoustic neurinomas and multiple subcutaneous…
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Review
1994
Review
1994
Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene.
Pierre Hutter
,
S. Antonarakis
,
C. D. Delozier-Blanchet
,
Michael A. Morris
Human Molecular Genetics
1994
Corpus ID: 26440799
Von Recklinghausen neurofibromatosis (neurofibromatosis type 1, NF1, McKusick no. 162200) is one of the most common human genetic…
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1992
1992
[A case of lung cancer in a patient with von Recklinghausen's disease].
K. Itoi
,
K. Yanagihara
,
K. Okubo
,
M. Kuwabara
Nihon Kyobu Shikkan Gakkai zasshi
1992
Corpus ID: 27972495
A 57-year-old man was admitted to our hospital for further investigation of an abnormal shadow in his chest X-ray. He had cafe-au…
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1992
1992
[Thoracic intramedullary neurinoma with multiple intracranial meningiomas; case report].
T. Morimoto
,
T. Sasaki
,
T. Mochizuki
,
K. Takakura
,
A. Sato
No shinkei geka. Neurological surgery
1992
Corpus ID: 22609885
A 42-year-old man suffered from numbness in his right leg in May, 1989, and was admitted to another hospital for examination…
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1985
1985
Urologic manifestations of von Recklinghausen neurofibromatosi
M. D. Blum
,
R. Bahnson
,
M. Carter
1985
Corpus ID: 58714395
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