Page last updated: 2024-10-18

glycine and Bilateral Deafness

glycine has been researched along with Bilateral Deafness in 2 studies

Research Excerpts

ExcerptRelevanceReference
"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."1.32Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene. ( Assadi, F; Brackbill, EL, 2003)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Assadi, F1
Brackbill, EL1
Syal, R1
Reddy S, J1
Kumar, R1
Tyagi, I1
Abrar, AA1
Krishnani, N1
Mishra, AM1
Gupta, RK1

Other Studies

2 other studies available for glycine and Bilateral Deafness

ArticleYear
Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2003, Volume: 41, Issue:1

    Topics: Adrenal Gland Neoplasms; Amino Acid Substitution; Child; Cryptorchidism; Developmental Disabilities;

2003
Unusual clinical and MRI features of a cerebellopontine angle medulloepithelioma. Case report and review of literature.
    Pediatric neurosurgery, 2006, Volume: 42, Issue:5

    Topics: Brain Chemistry; Cerebellar Neoplasms; Cerebellopontine Angle; Child, Preschool; Choline; Creatine;

2006