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SLC1A3 C3590T but not BDNF G196A is a predisposition factor for stress as well as depression, in an adolescent eastern Indian population

• Authors : Madhumita Ghosh; Akhtar Ali; Shobhna Joshi

Subjects: Depression; Stress; Adolescent

• Source: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)

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SLC1A3 C3590T but not BDNF G196A is a predisposition factor for stress as well as depression, in an adolescent eastern Indian population.

• Authors : Ghosh, Madhumita¹ (AUTHOR); Ali, Akhtar² (AUTHOR); Joshi, Shobhna³ (AUTHOR)

• Source: BMC Medical Genetics. 3/14/2020, Vol. 21 Issue 1, p1-10. 10p.

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Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report

• Authors : Kye Hee Cho; Sung Han Shim; Youngsoo Jung

Subjects: Neurodegeneration; Sjogren-Larsson syndrome; Dystonia

• Source: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)

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Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report.

• Authors : Cho KH; Department of Rehabilitation Medicine, CHA Bundang Medical Center, CHA University, 59 Yatap-ro, Bundang-gu, Seongnam, Gyeonggi-do, 13496, Republic of Korea.; Shim SH

Subjects: Neurodegenerative Diseases/Neurodegenerative Diseases/Neurodegenerative Diseases/*genetics ; Sjogren-Larsson Syndrome/Sjogren-Larsson Syndrome/Sjogren-Larsson Syndrome/*genetics; Adolescent

• Source: BMC medical genetics [BMC Med Genet] 2018 Aug 29; Vol. 19 (1), pp. 152. Date of Electronic Publication: 2018 Aug 29.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.

• Source: BMC Medical Genetics. 2011, Vol. 12 Issue 1, p92-98. 7p.

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Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report

• Authors : Sung Han Shim; Kye Hee Cho; Se Ra Sung

Subjects: 0301 basic medicine; lcsh:Internal medicine; Pediatrics

• Source: BMC Medical GeneticsBMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)

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Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.

• Authors : McGregor TL; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA. ; Gurnett CA

Subjects: Protein-Lysine 6-Oxidase/Protein-Lysine 6-Oxidase/Protein-Lysine 6-Oxidase/*genetics ; Scoliosis/Scoliosis/Scoliosis/*genetics; Adolescent

• Source: BMC medical genetics [BMC Med Genet] 2011 Jul 08; Vol. 12, pp. 92. Date of Electronic Publication: 2011 Jul 08.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents.

• Authors : Della Torre OH; Department of Psychiatry - Faculty of Medical Sciences (FCM), State University of Campinas (Unicamp), Campinas, SP, Brazil. .; Rua Tessália Vieira de Camargo, 126, Cidade Universitária Zeferino Vaz - Campinas, São Paulo, ZIP Code: 13083-887, Brazil. .

Subjects: Emotions* ; Polymorphism, Single Nucleotide*; Adolescent Behavior/Adolescent Behavior/Adolescent Behavior/*psychology

• Source: BMC medical genetics [BMC Med Genet] 2018 May 02; Vol. 19 (1), pp. 65. Date of Electronic Publication: 2018 May 02.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype

• Authors : Wise Carol A; Dobbs Matthew B; Gurnett Christina A

Subjects: Internal medicine; RC31-1245; Genetics

• Source: BMC Medical Genetics, Vol 12, Iss 1, p 92 (2011)

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Recurrent secondary genomic alterations in desmoplastic small round cell tumors.

• Authors : Chow, Warren A; Yee, Jiing-Kuan; Tsark, Walter

Subjects: Humans; Neoplasm Recurrence; Local

• Source: BMC medical genetics. 21(1)

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