Publications: Dr Uttara Kurup
Kurup U, Lim DBN, Maharaj AV, Ishida M, Davies JH, Storr HL
(
2025
)
.
Silver-Russell syndrome secondary to rare (epi)genotypes exhibits phenotypic heterogeneity challenging clinical diagnosis
.
Clinical Epigenetics
vol.
17
,
(
1
)
Palau H, Kurup U, N. LDB, Ishida M, Maharaj AV, Davies JH, Storr HL
(
2024
)
.
Rare causes of silver-russell syndrome frequently present with atypical features highlighting important implications for genetic testing and clinical management
.
Endocrine Abstracts
Palau H, Kurup U, Ishida M, Maharaj AV, Davies JH, Storr HL
(
2024
)
.
6890 The standard clinical diagnostic criteria for Silver-Russell Syndrome poorly identifies monogenic cases
.
Conference:
British Society of Paediatric Endocrinology and Diabetesa240.1
-
a2a240
.
Kurup U, Lim DBN, Palau H, Maharaj AV, Ishida M, Davies JH, Storr HL
(
2024
)
.
Approach to the Patient With Suspected Silver-Russell Syndrome
.
The Journal of Clinical Endocrinology & Metabolism
vol.
109
,
(
10
)
e1889
-
e1901
.
Kurup U, Palau H, Lim D, Ishida M, Vickram MA, Massoud A, Davies J, Storr H
(
2024
)
.
The expanding phenotypic spectrum of silver-russell syndrome may confound decisions to investigate for (epi)genetic causes
.
Endocrine Abstracts
Palau H, Kurup U, Ishida M, Maharaj AV, Davies JH, Storr HL
(
2023
)
.
Standard clinical diagnostic criteria for Silver-Russell Syndrome frequently overlooks monogenic causes
.
Endocrine Abstracts