glycine has been researched along with MEA 2a in 5 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Multiple endocrine neoplasia type 2A (MEN2A) is an autosomal dominant hereditary disorder, associated with a cluster of germline gain-of-function mutations of the RET proto-oncogene (RET), mainly in exons 10-15." | 2.44 | Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene. ( Boutati, E; Economopoulos, T; Hadjidakis, D; Kamakari, S; Panayiotides, IG; Peppa, M; Peros, G; Pikounis, V; Raptis, SA, 2008) |
| "The observed constellation of microcephaly, deafness, cryptorchidism, developmental delay, hypertension, and bilateral pheochromocytoma in association with a VHL mutation A451G in a patient with negative family history has not previously been described in the literature." | 1.32 | Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene. ( Assadi, F; Brackbill, EL, 2003) |
| "The association of multiple endocrine neoplasia type 2A with the dermatological disorder cutaneous lichen amyloidosis has already been reported, and mutations in the Cys634 have been identified in different families." | 1.30 | A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis. ( Betsos, N; Camera, G; Celli, I; Claudiani, F; Romeo, G; Seri, M, 1997) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Signorini, PS | 1 |
| França, MI | 1 |
| Camacho, CP | 1 |
| Lindsey, SC | 1 |
| Valente, FO | 1 |
| Kasamatsu, TS | 1 |
| Machado, AL | 1 |
| Salim, CP | 1 |
| Delcelo, R | 1 |
| Hoff, AO | 1 |
| Cerutti, JM | 1 |
| Dias-da-Silva, MR | 1 |
| Maciel, RM | 1 |
| Lang, BH | 1 |
| Yu, HW | 1 |
| Lo, CY | 1 |
| Lee, KE | 1 |
| Garcia-Barcelo, MM | 1 |
| Woo, YC | 1 |
| Lee, PC | 1 |
| Wong, KP | 1 |
| Tam, PK | 1 |
| Lam, KS | 1 |
| Peppa, M | 1 |
| Boutati, E | 1 |
| Kamakari, S | 1 |
| Pikounis, V | 1 |
| Peros, G | 1 |
| Panayiotides, IG | 1 |
| Economopoulos, T | 1 |
| Raptis, SA | 1 |
| Hadjidakis, D | 1 |
| Assadi, F | 1 |
| Brackbill, EL | 1 |
| Seri, M | 1 |
| Celli, I | 1 |
| Betsos, N | 1 |
| Claudiani, F | 1 |
| Camera, G | 1 |
| Romeo, G | 1 |
1 review available for glycine and MEA 2a
| Article | Year |
|---|---|
Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Carcinoma, Medullary; Cysteine; Female; Gly | 2008 |
4 other studies available for glycine and MEA 2a
| Article | Year |
|---|---|
A ten-year clinical update of a large RET p.Gly533Cys kindred with medullary thyroid carcinoma emphasizes the need for an individualized assessment of affected relatives.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Calcitonin; Carcinoembryonic Antigen; Carcinoma, N | 2014 |
Bilateral Pheochromocytomas in MEN2A Syndrome: A Two-Institution Experience.
Topics: Adolescent; Adrenal Gland Neoplasms; Adrenalectomy; Adult; Age Factors; Aged; Aged, 80 and over; Ami | 2015 |
Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene.
Topics: Adrenal Gland Neoplasms; Amino Acid Substitution; Child; Cryptorchidism; Developmental Disabilities; | 2003 |
A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.
Topics: Adolescent; Adult; Amyloidosis; Child; Cysteine; Deoxyribonucleases, Type II Site-Specific; Drosophi | 1997 |