-
2
-
-
33645604309
-
Epidemiology of child and adolescent mental health problems and mental retardation
-
Srinath S, Girimaji SR. Epidemiology of child and adolescent mental health problems and mental retardation. NIMHANS J 1999; 17:355-366.
-
(1999)
NIMHANS J
, vol.17
, pp. 355-366
-
-
Srinath, S.1
Girimaji, S.R.2
-
3
-
-
24044546788
-
Epidemiological study of child & adolescent psychiatric disorders in urban & rural areas of Bangalore, India
-
Srinath S, Girimaji SC, Gururaj G, et al. Epidemiological study of child & adolescent psychiatric disorders in urban & rural areas of Bangalore, India. Indian J Med Res 2005; 122:67-79.
-
(2005)
Indian J Med Res
, vol.122
, pp. 67-79
-
-
Srinath, S.1
Girimaji, S.C.2
Gururaj, G.3
-
4
-
-
22344440186
-
A community genetics approach to population screening in India for mental retardation: A model for developing countries
-
Dave U, Shetty N, Mehta L. A community genetics approach to population screening in India for mental retardation: A model for developing countries. Ann Hum Biol 2005; 32:195-203.
-
(2005)
Ann Hum Biol
, vol.32
, pp. 195-203
-
-
Dave, U.1
Shetty, N.2
Mehta, L.3
-
5
-
-
4644355478
-
Prevalence of neurological disorders in Bangalore, India: A community-based study with a comparison between urban and rural areas
-
Gourie-Devi M, Gururaj G, Satishchandra P, Subbakrishna DK. Prevalence of neurological disorders in Bangalore, India: A community-based study with a comparison between urban and rural areas. Neuroepidemiology 2004; 23:261-268.
-
(2004)
Neuroepidemiology
, vol.23
, pp. 261-268
-
-
Gourie-Devi, M.1
Gururaj, G.2
Satishchandra, P.3
Subbakrishna, D.K.4
-
6
-
-
0026149392
-
ICMR Collaborating Centres & Central Co-ordinating Unit. Multicentric study on genetic causes of mental retardation in India
-
ICMR Collaborating Centres & Central Co-ordinating Unit. Multicentric study on genetic causes of mental retardation in India. Indian J Med Res 1991; 94:161-169.
-
(1991)
Indian J Med Res
, vol.94
, pp. 161-169
-
-
-
14
-
-
77955469645
-
Clinical practice guidelines for the diagnosis and management of children with mental retardation. Bangalore
-
A good summary of the way to go about caring for persons with mental retardation in the Indian context
-
Girimaji SC. Clinical practice guidelines for the diagnosis and management of children with mental retardation. Bangalore: NIMHANS; 2008. www.indianj psychiatry.org/cpg/cpg2008/CPG-CAP-05.pdf. A good summary of the way to go about caring for persons with mental retardation in the Indian context.
-
(2008)
NIMHANS
-
-
Girimaji, S.C.1
-
16
-
-
77955470626
-
-
Government of India. Sarva Shiksha Abhiyan. Department of School Education and Literacy, Ministry of Human Resource Development
-
Government of India. Sarva Shiksha Abhiyan. Department of School Education and Literacy, Ministry of Human Resource Development; 2007. http://ssa.nic.in/.
-
(2007)
-
-
-
18
-
-
84978345610
-
Family focused intervention in mental retardation: Indian models
-
In: Bhatti RS, Varghese M, Raguram A, editors., Bangalore: NIMHANS
-
Girimaji SR. Family focused intervention in mental retardation: Indian models. In: Bhatti RS, Varghese M, Raguram A, editors. Changing marital and family systems: Challenges to conventional models in mental health. Bangalore: NIMHANS; 2003. pp. 192-199.
-
(2003)
Changing Marital and Family Systems: Challenges to Conventional Models in Mental Health
, pp. 192-199
-
-
Girimaji, S.R.1
-
19
-
-
0033050585
-
Family intervention for intellectually disabled children. randomised controlled trial
-
Russell PSS, John JK, Lakshmanan JL. Family intervention for intellectually disabled children. Randomised controlled trial. Br J Psychiatry 1999; 174:254-258.
-
(1999)
Br J Psychiatry
, vol.174
, pp. 254-258
-
-
Russell, P.S.S.1
John, J.K.2
Lakshmanan, J.L.3
-
20
-
-
77955469363
-
Family Interview for Stress and Coping in Mental Retardation [FISC-MR]: A tool to study stress and coping in families of children with mental retardation
-
Girimaji SC, Srinath S, Seshadri SP, Subbakrishna DK. Family Interview for Stress and Coping in Mental Retardation [FISC-MR]: A tool to study stress and coping in families of children with mental retardation. Indian J Psychiatry 1999; 41:341-349.
-
(1999)
Indian J Psychiatry
, vol.41
, pp. 341-349
-
-
Girimaji, S.C.1
Srinath, S.2
Seshadri, S.P.3
Subbakrishna, D.K.4
-
21
-
-
33846959775
-
A review of community based rehabilitation evaluations: Quality of life as an outcome measure for future evaluations
-
Mannan H, Turnbull AP. A review of community based rehabilitation evaluations: quality of life as an outcome measure for future evaluations. Asia Pac Disabil Rehabil J 2007; 18:29-45.
-
(2007)
Asia Pac Disabil Rehabil J
, vol.18
, pp. 29-45
-
-
Mannan, H.1
Turnbull, A.P.2
-
23
-
-
77949757570
-
Newborn screening in India: Current perspectives
-
This article reviews the evidence for initiating neonatal screening for hypothyroidism in India
-
Kapoor S, Kabra M. Newborn screening in India: Current perspectives. Indian Pediatr 2010; 47:219-224. This article reviews the evidence for initiating neonatal screening for hypothyroidism in India.
-
(2010)
Indian Pediatr
, vol.47
, pp. 219-224
-
-
Kapoor, S.1
Kabra, M.2
-
24
-
-
77955469277
-
Government of India. broad framework for preparation of district health action plans
-
Government of India. Broad Framework for Preparation of District Health Action Plans. National Rural Health Mission; 2010. http://mohfw.nic.in/NRHM/RCH/ Index.htm.
-
(2010)
National Rural Health Mission
-
-
-
25
-
-
77955473353
-
Government of India. Integrated child development services (ICDS) scheme
-
Government of India. Integrated Child Development Services (ICDS) Scheme. Ministry of Women and Child Development; 2009. http://wcd.nic. in/icds.htm.
-
(2009)
Ministry of Women and Child Development
-
-
-
26
-
-
62649118818
-
Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly
-
This article describes a new mutated gene in primary microcephaly, a condition not very rare in south India
-
Kumar A, Girimaji SC, Duvvari MR, Blanton SH. Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. Am J Hum Genet 2009; 84:286-290. This article describes a new mutated gene in primary microcephaly, a condition not very rare in south India.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 286-290
-
-
Kumar, A.1
Girimaji, S.C.2
Duvvari, M.R.3
Blanton, S.H.4
-
27
-
-
74349103977
-
Screening of rural children in West Bengal for fragile-X syndrome
-
This study reports on findings of population-based screening for fragile X syndrome
-
Dutta S, Das M, Bhowmik AD, et al. Screening of rural children in West Bengal for fragile-X syndrome. Indian J Med Res 2009; 130:714-719. This study reports on findings of population-based screening for fragile X syndrome.
-
(2009)
Indian J Med Res
, vol.130
, pp. 714-719
-
-
Dutta, S.1
Das, M.2
Bhowmik, A.D.3
-
28
-
-
70849131938
-
Use of multiplex ligation-dependent probe amplification [MLPA] in screening of subtelomeric regions in children with idiopathic mental retardation
-
This is one of the first studies investigating subtelomeric alterations from India
-
Mandal K, Boggula VR, Borkar M, et al. Use of multiplex ligation-dependent probe amplification [MLPA] in screening of subtelomeric regions in children with idiopathic mental retardation. Indian J Pediatr 2009; 76:1027-1031. This is one of the first studies investigating subtelomeric alterations from India.
-
(2009)
Indian J Pediatr
, vol.76
, pp. 1027-1031
-
-
Mandal, K.1
Boggula, V.R.2
Borkar, M.3
-
29
-
-
68949097521
-
Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India
-
This study reports a method to improve the detection rate of fragile X syndrome
-
Guruju MR, Lavanya K, Thelma BK, et al. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India. J Clin Neurosci 2009; 16:1305-1310. This study reports a method to improve the detection rate of fragile X syndrome.
-
(2009)
J Clin Neurosci
, vol.16
, pp. 1305-1310
-
-
Guruju, M.R.1
Lavanya, K.2
Thelma, B.K.3
-
30
-
-
67650086714
-
Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: Report of two classical Rett syndrome patients of Indian origin
-
This study reports a simple molecular genetic method to detect the most common mutations in Rett syndrome
-
Khajuria R, Sapra S, Ghosh M, et al. Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: Report of two classical Rett syndrome patients of Indian origin. Genet Test Mol Biomarkers 2009; 13:277-280. This study reports a simple molecular genetic method to detect the most common mutations in Rett syndrome.
-
(2009)
Genet Test Mol Biomarkers
, vol.13
, pp. 277-280
-
-
Khajuria, R.1
Sapra, S.2
Ghosh, M.3
-
33
-
-
67650918321
-
Needs of Indian parents having children with intellectual disability
-
This study explores the needs of parents of children with intellectual disability at different ages
-
Verma RK, Kishore MT. Needs of Indian parents having children with intellectual disability. Int J Rehabil Res 2009; 32:71-76. This study explores the needs of parents of children with intellectual disability at different ages.
-
(2009)
Int J Rehabil Res
, vol.32
, pp. 71-76
-
-
Verma, R.K.1
Kishore, M.T.2
-
34
-
-
71649094499
-
Living with a developmentally disabled child: Attitude of family members in India
-
This study employs qualitative approach to understand families of children with developmental disabilities
-
Dhar RL. Living with a developmentally disabled child: Attitude of family members in India. Social Sci J 2009; 46:738-755. This study employs qualitative approach to understand families of children with developmental disabilities.
-
(2009)
Social Sci J
, vol.46
, pp. 738-755
-
-
Dhar, R.L.1
-
35
-
-
33644864462
-
The determinants of compliance with an early intervention programme for high-risk babies in India
-
De Souza N, Sardessai V, Joshi K, et al. The determinants of compliance with an early intervention programme for high-risk babies in India. Child Care Health Dev 2006; 32:63-72.
-
(2006)
Child Care Health Dev
, vol.32
, pp. 63-72
-
-
De Souza, N.1
Sardessai, V.2
Joshi, K.3
-
36
-
-
33746669362
-
Early intervention in developmental delay
-
Kaur P, Chavan BS, Lata S, et al. Early intervention in developmental delay. Indian J Pediatr 2006; 73:405-408.
-
(2006)
Indian J Pediatr
, vol.73
, pp. 405-408
-
-
Kaur, P.1
Chavan, B.S.2
Lata, S.3
-
37
-
-
66149088110
-
Hypoxic ischemic encephalopathy developmental outcome at 12 years
-
George B, Padmam MS, Nair MK, et al. Hypoxic ischemic encephalopathy developmental outcome at 12 years. Indian Pediatr 2009; 46 (Suppl): S67-s70.
-
(2009)
Indian Pediatr
, vol.46
, Issue.SUPPL.
-
-
George, B.1
Padmam, M.S.2
Nair, M.K.3
-
38
-
-
34447130152
-
Childhood disability in low- and middle-income countries: Overview of screening, prevention, services, legislation, and epidemiology
-
Maulik PK, Darmstadt GL. Childhood disability in low- and middle-income countries: Overview of screening, prevention, services, legislation, and epidemiology. Pediatrics 2007; 120:S1-S55.
-
(2007)
Pediatrics
, vol.120
-
-
Maulik, P.K.1
Darmstadt, G.L.2
|