Neurofibromatosis Type 1-Noonan Syndrome: What’s the Link?

Noonan Syndrome ◽

Pheochromocytoma Associated with Neurofibromatosis Type 1 and Noonan Syndrome: A Case Report and Literature Review

Biomedical Journal of Scientific & Technical Research ◽

10.26717/bjstr.2020.31.005066 ◽

2020 ◽

Vol 31 (2) ◽

Author(s):

Sana Abid

Keyword(s):

Case Report ◽

Literature Review ◽

Noonan Syndrome ◽

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association

American Journal of Medical Genetics ◽

10.1002/(sici)1096-8628(19961218)66:3<347::aid-ajmg20>3.0.co;2-l ◽

1996 ◽

Vol 66 (3) ◽

pp. 347-355 ◽

Cited By ~ 19

Author(s):

Michel Bahuau ◽

Wayne Flintoff ◽

Brigitte Assouline ◽

Stanislas Lyonnet ◽

Martine Le Merrer ◽

...

Keyword(s):

Noonan Syndrome ◽

Large Family ◽

Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus

Clinical Genetics ◽

10.1111/j.1399-0004.1995.tb04061.x ◽

2008 ◽

Vol 48 (2) ◽

pp. 85-89 ◽

Cited By ~ 17

Author(s):

Bodil Edman Ahlbom ◽

Niklas Dahl ◽

Per Zetterqvist ◽

Goran Annerén

Keyword(s):

Noonan Syndrome ◽

Neurofibromatosis Type ◽

Café Au Lait Spots ◽

Multiple Lentigines

Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome

American Journal of Medical Genetics ◽

10.1002/(sici)1096-8628(19980123)75:3<265::aid-ajmg8>3.0.co;2-p ◽

1998 ◽

Vol 75 (3) ◽

pp. 265-272 ◽

Cited By ~ 25

Author(s):

Michel Bahuau ◽

Claude Houdayer ◽

Brigitte Assouline ◽

Claudine Blanchet-Bardon ◽

Martine Le Merrer ◽

...

Keyword(s):

Noonan Syndrome ◽

Nonsense Mutation ◽

Emotional functioning among children with neurofibromatosis type 1 or Noonan syndrome

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.61361 ◽

2019 ◽

Vol 179 (12) ◽

pp. 2433-2446 ◽

Cited By ~ 1

Author(s):

Alana M. McNeill ◽

Rebekah L. Hudock ◽

Allison M. H. Foy ◽

Ryan Shanley ◽

Margaret Semrud‐Clikeman ◽

...

Keyword(s):

Noonan Syndrome ◽

Emotional Functioning ◽

Diffuse-type Tenosynovial Giant Cell Tumor in Association With Neurofibromatosis Type 1-Noonan Syndrome: Possibly More Than a Chance Relationship

The American Journal of Surgical Pathology ◽

10.1097/00000478-200606000-00009 ◽

2006 ◽

Vol 30 (6) ◽

pp. 734-738 ◽

Cited By ~ 2

Author(s):

Lorena Posligua ◽

Douglas J. McDonald ◽

Louis P. Dehner

Keyword(s):

Giant Cell Tumor ◽

Giant Cell ◽

Noonan Syndrome ◽

Neurofibromatosis Type ◽

Cell Tumor ◽

Diffuse Type ◽

Tenosynovial Giant Cell Tumor

Novel association of neurofibromatosis type 1-causing mutations in families with neurofibromatosis-noonan syndrome

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.36313 ◽

2013 ◽

Vol 164 (3) ◽

pp. 579-587 ◽

Cited By ~ 16

Author(s):

Sara Ekvall ◽

Kerstin Sjörs ◽

Anders Jonzon ◽

Mauno Vihinen ◽

Göran Annerén ◽

...

Keyword(s):

Noonan Syndrome ◽

Neurofibromatosis Type ◽

Novel Association

Social skills in children with RASopathies: a comparison of Noonan syndrome and neurofibromatosis type 1

Journal of Neurodevelopmental Disorders ◽

10.1186/s11689-018-9239-8 ◽

2018 ◽

Vol 10 (1) ◽

Cited By ~ 6

Author(s):

Elizabeth I. Pierpont ◽

Rebekah L. Hudock ◽

Allison M. Foy ◽

Margaret Semrud-Clikeman ◽

Mary Ella Pierpont ◽

...

Keyword(s):

Social Skills ◽

Noonan Syndrome ◽

Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.

Journal of Medical Genetics ◽

10.1136/jmg.29.3.188 ◽

1992 ◽

Vol 29 (3) ◽

pp. 188-190 ◽

Cited By ~ 21

Author(s):

M Sharland ◽

R Taylor ◽

M A Patton ◽

S Jeffery

Keyword(s):

Noonan Syndrome ◽

Patient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome

Clinical Dysmorphology ◽

10.1097/mcd.0b013e3283557231 ◽

2012 ◽

Vol 21 (4) ◽

pp. 212-214 ◽

Cited By ~ 4

Author(s):

Ellen A. Croonen ◽

Helger G. Yntema ◽

Rick van Minkelen ◽

Ans M.W. van den Ouweland ◽

Ineke van der Burgt

Keyword(s):

Clinical Diagnosis ◽

Noonan Syndrome ◽