-
1
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 2001; 29:465-8.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
Zampino, G.4
Brunner, H.G.5
Kremer, H.6
-
2
-
-
0028077697
-
Mapping a gene for Noonan syndrome to the long arm of chromosome 12
-
Jamieson CR, Van Der Burgt I, Brady AF, van Reen M, Elsawi MM, Hol F et al. Mapping a gene for Noonan syndrome to the long arm of chromosome 12. Nat Genet 1994; 8:357-60.
-
(1994)
Nat Genet
, vol.8
, pp. 357-360
-
-
Jamieson, C.R.1
Van Der Burgt, I.2
Brady, A.F.3
van Reen, M.4
Elsawi, M.M.5
Hol, F.6
-
3
-
-
0033186306
-
-
Bertola DR, Sugayama SM, Albano LM, Kim CA, Gonzalez CH. Noonan syndrome: a clinical and genetic study of 31 patients. Rev Hospital Clin Fac Med Sao Paulo 1999; 54:147-50.
-
Bertola DR, Sugayama SM, Albano LM, Kim CA, Gonzalez CH. Noonan syndrome: a clinical and genetic study of 31 patients. Rev Hospital Clin Fac Med Sao Paulo 1999; 54:147-50.
-
-
-
-
4
-
-
0027993959
-
Noonan syndrome: An update and review for the primary pediatrician
-
Noonan JA. Noonan syndrome: an update and review for the primary pediatrician. Clin Pediatr (Phila) 1994; 33:548-55.
-
(1994)
Clin Pediatr (Phila)
, vol.33
, pp. 548-555
-
-
Noonan, J.A.1
-
6
-
-
2342642111
-
Aneurysmal sub-arachnoid haemorrhage in patients with Noonan syndrome: A report of two cases and review of neurovascular presentations in this syndrome
-
Dineen RA, Lenthall RK. Aneurysmal sub-arachnoid haemorrhage in patients with Noonan syndrome: a report of two cases and review of neurovascular presentations in this syndrome. Neuroradiology 2004; 46:301-5.
-
(2004)
Neuroradiology
, vol.46
, pp. 301-305
-
-
Dineen, R.A.1
Lenthall, R.K.2
-
7
-
-
0027500062
-
Noonan phenotype associated with intracerebral hemorrhage and cerebrovascular anomalies: Case report
-
Hara T, Sasaki T, Miyauchi H, Takakura K. Noonan phenotype associated with intracerebral hemorrhage and cerebrovascular anomalies: case report. Surg Neurol 1993; 39:31-6.
-
(1993)
Surg Neurol
, vol.39
, pp. 31-36
-
-
Hara, T.1
Sasaki, T.2
Miyauchi, H.3
Takakura, K.4
-
8
-
-
0026567389
-
Cerebral arteriovenous malformation in Noonan's syndrome
-
Schon F, Bowler J, Baraitser M. Cerebral arteriovenous malformation in Noonan's syndrome. Postgrad Med J 1992; 68:37-40.
-
(1992)
Postgrad Med J
, vol.68
, pp. 37-40
-
-
Schon, F.1
Bowler, J.2
Baraitser, M.3
-
9
-
-
0029652826
-
Noonan syndrome associated with thromboembolic brain infarcts and posterior circulation abnormalities
-
Hinnant CA. Noonan syndrome associated with thromboembolic brain infarcts and posterior circulation abnormalities. Am J Med Genet 1995; 56:241-4.
-
(1995)
Am J Med Genet
, vol.56
, pp. 241-244
-
-
Hinnant, C.A.1
-
11
-
-
33947222780
-
-
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders, 2nd edn. Cephalalgia 2004; 24 (Suppl. 1):1-160.
-
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders, 2nd edn. Cephalalgia 2004; 24 (Suppl. 1):1-160.
-
-
-
-
12
-
-
0036788832
-
The first Noonan syndrome gene: PTPN11, which encodes the protein tyrosine phosphatase SHP-2
-
Allanson J. The first Noonan syndrome gene: PTPN11, which encodes the protein tyrosine phosphatase SHP-2. Pediatr Res 2002; 52 (4):471.
-
(2002)
Pediatr Res
, vol.52
, Issue.4
, pp. 471
-
-
Allanson, J.1
-
13
-
-
18344370436
-
PTPN11 mutations in Noonan syndrome: Molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity
-
Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I et al. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet 2002; 70:1555-63.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1555-1563
-
-
Tartaglia, M.1
Kalidas, K.2
Shaw, A.3
Song, X.4
Musat, D.L.5
van der Burgt, I.6
-
14
-
-
0019946801
-
Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome
-
Peiris A, Ball MJ. Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome. J Neurol Neurosurg Psychiatry 1982; 45:753-4.
-
(1982)
J Neurol Neurosurg Psychiatry
, vol.45
, pp. 753-754
-
-
Peiris, A.1
Ball, M.J.2
-
15
-
-
0000450546
-
Migraine and headache: A meta-analytic approach
-
Crombie I, ed, Seattle: IASP Press
-
Scher AI, Stewart WF, Lipton RB. Migraine and headache: a meta-analytic approach. In: Crombie I, ed. Epidemiology of Pain. Seattle: IASP Press, 1999:59-70.
-
(1999)
Epidemiology of Pain
, pp. 59-70
-
-
Scher, A.I.1
Stewart, W.F.2
Lipton, R.B.3
-
16
-
-
33644943390
-
Patterns of medical diagnosis and treatment of migraine and probable migraine in a health plan
-
Bigal ME, Kolodner KB, Lafata JE, Leotta C, Lipton RB. Patterns of medical diagnosis and treatment of migraine and probable migraine in a health plan. Cephalalgia 2006; 26:43-9.
-
(2006)
Cephalalgia
, vol.26
, pp. 43-49
-
-
Bigal, M.E.1
Kolodner, K.B.2
Lafata, J.E.3
Leotta, C.4
Lipton, R.B.5
|