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Co-authors
(41)
Maria I. New
22
Karen Lin-Su
10
Robert B. Wilson
7
Ken McElreavey
3
Giovanna Vinci
3
Journals
(15)
J CLIN ENDOCRINOL METAB
4
TRENDS ENDOCRINOL METAB
2
J PEDIAT
2
MOL GENET METAB
2
ANN N Y ACAD SCI
2
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Authors
Saroj Nimkarn
Saroj Nimkarn,Mount Sinai Medical Center & School of Medicine,Endocrinology,Molecular Biology,Genetics & Genealogy
Edit
Saroj Nimkarn
Mount Sinai Medical Center & School of Medicine
Publications:
27
|
Citations:
109
Fields:
Endocrinology
,
Molecular Biology
,
Genetics & Genealogy
View FAQ about top research areas and Fields of study
Collaborated with
41 co-authors
from 1999 to 2011
|
Cited by
401 authors
Cumulative
Annual
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Publications
(27)
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Steroid 21 Hydroxylase Deficiency Congenital Adrenal Hyperplasia
Saroj Nimkarn
,
Karen Lin-Su
,
Maria I. New
Journal:
Pediatric Clinics of North America - PEDIAT CLIN N AMER
, vol. 58, no. 5, pp. 1281-1300, 2011
Resistance to Several Steroids in Two Sisters
(
Citations: 8
)
M. I. NEW
,
S. NIMKARN
,
D. D. BRANDON
,
S. CUNNINGHAM-RUNDLES
,
R. C. WILSON
,
R. S. NEWFIELD
,
J. VANDERMEULEN
,
N. BARRON
,
C. RUSSO
,
D. L. LORIAUX
,
B. O'MALLEY
Published in 2010.
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Saroj Nimkarn
,
Maria I. New
Journal:
Annals of The New York Academy of Sciences - ANN N Y ACAD SCI
, vol. 1192, no. 1, pp. 5-11, 2010
Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
(
Citations: 7
)
Saroj Nimkarn
,
Maria I. New
Journal:
Molecular and Cellular Endocrinology - MOL CELL ENDOCRINOL
, vol. 300, no. 1, pp. 192-196, 2009
Steroid 21 Hydroxylase Deficiency Congenital Adrenal Hyperplasia
(
Citations: 3
)
Saroj Nimkarn
,
Karen Lin-Su
,
Maria I. New
Journal:
Endocrinology and Metabolism Clinics of North America - ENDOCRINOL METAB CLIN N AMER
, vol. 38, no. 4, pp. 699-718, 2009
Sort by:
Citations
(109 times by 102 publications)
Peristaltic transport of fractional Maxwell fluids in uniform tubes: Applications in endoscopy
(
Citations: 1
)
Dharmendra Tripathi
Journal:
Computers & Mathematics With Applications - COMPUT MATH APPL
, vol. 62, no. 3, pp. 1116-1126, 2011
In Vivo Fate Mapping and Expression Analysis Reveals Molecular Hallmarks of Prospectively Isolated Adult Neural Stem Cells
Ruth Beckervordersandforth
,
Pratibha Tripathi
,
Jovica Ninkovic
,
Efil Bayam
,
Alexandra Lepier
,
Barbara Stempfhuber
,
Frank Kirchhoff
,
Johannes Hirrlinger
,
Anja Haslinger
,
D. Chichung Lie
,
Johannes Beckers
,
Bradley Yoder
http://academic.research.microsoft.com/io.ashx?type=5&id=49687780&selfId1=11114663&selfId2=0&maxNumber=12&query=
Journal:
Cell Stem Cell
, vol. 8, no. 1, pp. 119-119, 2011
Molecular Defects of the CYP21A2 Gene in Greek-Cypriot Patients with Congenital Adrenal Hyperplasia
Nicos Skordis
,
Andreas Kyriakou
,
Véronique Tardy
,
Yiannis S. Ioannou
,
Athanasia Varvaresou
,
Maria Dracopoulou-Vabouli
,
Philippos C. Patsalis
,
Christos Shammas
,
Vassos Neocleous
,
Leonidas A. Phylactou
Journal:
Hormone Research in Paediatrics
, vol. 75, pp. 180-186, 2011
Structure-Based Analysis of Five Novel Disease-Causing Mutations in 21-Hydroxylase-Deficient Patients
Carolina Minutolo
,
Alejandro D. Nadra
,
Cecilia Fernández
,
Melisa Taboas
,
Noemí Buzzalino
,
Bárbara Casali
,
Susana Belli
,
Eduardo H. Charreau
,
Liliana Alba
,
Liliana Dain
,
Claudine Mayer
Journal:
PLOS One
, vol. 6, no. 1, 2011
Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients
Aysha H Khan
,
Muniba Aban
,
Jamal Raza
,
Naeem ul Haq
,
Abdul Jabbar
,
Tariq Moatter
Journal:
BMC Endocrine Disorders - BMC Endocr Disord
, vol. 11, no. 1, pp. 1-6, 2011
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