Myeloproliferative Disease and Cancer in Persons with Noonan Syndrome and Related Disorders

Noonan Syndrome and Related Disorders - A Matter of Deregulated Ras Signaling - Monographs in Human Genetics ◽

10.1159/000164848 ◽

2008 ◽

pp. 119-127

Keyword(s):

Noonan Syndrome ◽

Myeloproliferative Disease

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C008 Clinical and molecular features in patients with juvenile myelomonocytic leukemia-like myeloproliferative disease and Noonan syndrome

Leukemia Research ◽

10.1016/s0145-2126(07)70046-2 ◽

2007 ◽

Vol 31 ◽

pp. S27

Author(s):

C.P. Kratz ◽

C.M. Niemeyer

Keyword(s):

Noonan Syndrome ◽

Juvenile Myelomonocytic Leukemia ◽

Myeloproliferative Disease ◽

Molecular Features ◽

Myelomonocytic Leukemia

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Sulforaphane Inhibits SHP2 to Provide Therapy Against Noonan Syndrome-Associated Myeloproliferative Disease

Free Radical Biology and Medicine ◽

10.1016/j.freeradbiomed.2019.10.099 ◽

2019 ◽

Vol 145 ◽

pp. S39

Keyword(s):

Noonan Syndrome ◽

Myeloproliferative Disease

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The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

Blood ◽

10.1182/blood-2005-02-0531 ◽

2005 ◽

Vol 106 (6) ◽

pp. 2183-2185 ◽

Cited By ~ 146

Author(s):

C. P. Kratz

Keyword(s):

Noonan Syndrome ◽

Juvenile Myelomonocytic Leukemia ◽

Myeloproliferative Disease ◽

Mutational Spectrum ◽

Myelomonocytic Leukemia

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Combined defect in membrane expression and activation of platelet GPIIb-IIIa complex without primary sequence abnormalities in myeloproliferative disease

British Journal of Haematology ◽

10.1046/j.1365-2141.2000.02444.x ◽

2000 ◽

Vol 111 (3) ◽

pp. 954-964 ◽

Cited By ~ 7

Author(s):

Robert Kaplan ◽

Jagadeesh Gabbeta ◽

Ling Sun ◽

Guang Fen Mao ◽

A. Koneti Rao

Keyword(s):

Myeloproliferative Disease ◽

Primary Sequence ◽

Membrane Expression

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Rare NRAS mutation causing Noonan syndrome type 6 in a Saudi patient: case report

International Journal of Medicine in Developing Countries ◽

10.24911/ijmdc.51-1608055911 ◽

2021 ◽

pp. 413-415

Author(s):

Sara Alomar ◽

Anfal Alsultan ◽

Halah AlMuhaidib ◽

Sarah Aldhahri ◽

Dalal Bubshait

Keyword(s):

Case Report ◽

Noonan Syndrome ◽

Syndrome Type ◽

Patient Case ◽

Nras Mutation

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THE CLINICAL COURSE AND CARDIAC CHARACTERISTICS OF CHILDREN WITH NOONAN SYNDROME AND HYPERTROPHIC CARDIOMYOPATHY DIFFER FROM CHILDREN WITH NON-SYNDROMIC FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

10.26226/morressier.57d034cfd462b80292383272 ◽

2016 ◽

Author(s):

Emanuel KALTENECKER

Keyword(s):

Hypertrophic Cardiomyopathy ◽

Noonan Syndrome ◽

Clinical Course ◽

Familial Hypertrophic Cardiomyopathy

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Pediatric Acute Onset Neuropsychiatric Syndrome Associated with Epstein-barr Infection in Child with Noonan Syndrome

10.26226/morressier.58d4fec5d462b8028d892233 ◽

2017 ◽

Author(s):

Giuseppe Pietro Tisi

Keyword(s):

Noonan Syndrome ◽

Acute Onset ◽

Epstein Barr

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Paradoxical gingival bleeding in patient with chronic myeloproliferative disease: a case report

10.26226/morressier.5ac3832a2afeeb00097a40fb ◽

2018 ◽

Author(s):

Larisa Musić

Keyword(s):

Case Report ◽

Myeloproliferative Disease ◽

Gingival Bleeding ◽

Chronic Myeloproliferative Disease

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Faculty Opinions recommendation of Germline KRAS mutations cause Noonan syndrome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1031214.368837 ◽

2006 ◽

Author(s):

Alfred Wittinghofer

Keyword(s):

Noonan Syndrome ◽

Kras Mutations

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Faculty Opinions recommendation of Germline gain-of-function mutations in RAF1 cause Noonan syndrome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1089084.542244 ◽

2007 ◽

Author(s):

Deborah Morrison

Keyword(s):

Noonan Syndrome ◽

Gain Of Function

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