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1
Respiratory failure caused by lipoid pneumonia from vaping e-cigarettes
Respiratory failure caused by lipoid pneumonia from vaping e-cigarettes
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Respiratory failure caused by lipoid pneumonia from vaping e-cigarettes

BMJ case reports, 2018-07, Vol.2018, p.bcr-2018-224350 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ. ;Copyright: 2018 © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ. ;BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ. 2018 ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2018-224350 ;PMID: 29982176

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2
Congenital cerebriform plaque in a newborn
Congenital cerebriform plaque in a newborn
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Congenital cerebriform plaque in a newborn

BMJ case reports, 2022-06, Vol.15 (6), p.e250974 [Peer Reviewed Journal]

2022 BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-250974 ;PMID: 35680282

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3
Pontine tegmental cap dysplasia: the role of diffusion tensor imaging
Pontine tegmental cap dysplasia: the role of diffusion tensor imaging
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Pontine tegmental cap dysplasia: the role of diffusion tensor imaging

BMJ case reports, 2023-11, Vol.16 (11), p.e253556 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-253556

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4
Whole exome sequencing, clinical exome or targeted gene panels: what to choose for suspected lethal skeletal dysplasia (short rib thoracic dysplasia type IV)
Whole exome sequencing, clinical exome or targeted gene panels: what to choose for suspected lethal skeletal dysplasia (short rib thoracic dysplasia type IV)
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Whole exome sequencing, clinical exome or targeted gene panels: what to choose for suspected lethal skeletal dysplasia (short rib thoracic dysplasia type IV)

BMJ case reports, 2022-09, Vol.15 (9), p.e251118 [Peer Reviewed Journal]

2022 BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-251118

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5
Congenital smooth muscle hamartoma: an atypical presentation
Congenital smooth muscle hamartoma: an atypical presentation
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Congenital smooth muscle hamartoma: an atypical presentation

BMJ case reports, 2022-11, Vol.15 (11), p.e252240 [Peer Reviewed Journal]

2022 BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-252240

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6
Early recognition of unilateral absence of sternocleidomastoid muscle in a newborn presenting with contralateral congenital torticollis
Early recognition of unilateral absence of sternocleidomastoid muscle in a newborn presenting with contralateral congenital torticollis
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Early recognition of unilateral absence of sternocleidomastoid muscle in a newborn presenting with contralateral congenital torticollis

BMJ case reports, 2023-12, Vol.16 (12), p.e258532 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-258532 ;PMID: 38154876

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7
Diagnosing congenital hypochromic patches
Diagnosing congenital hypochromic patches
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Diagnosing congenital hypochromic patches

BMJ case reports, 2023-12, Vol.16 (12), p.e258827 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-258827 ;PMID: 38123319

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8
Regenerative nodules as harbinger of Abernethy malformation
Regenerative nodules as harbinger of Abernethy malformation
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Regenerative nodules as harbinger of Abernethy malformation

BMJ case reports, 2023-12, Vol.16 (12), p.e258634 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-258634 ;PMID: 38061860

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9
Atypical hypertrophy of retinal pigment epithelium manifesting as the first sign of familial adenomatous polyposis
Atypical hypertrophy of retinal pigment epithelium manifesting as the first sign of familial adenomatous polyposis
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Atypical hypertrophy of retinal pigment epithelium manifesting as the first sign of familial adenomatous polyposis

BMJ case reports, 2023-11, Vol.16 (11), p.e254350 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-254350

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10
Unravelling the complexity of heterotaxy syndrome
Unravelling the complexity of heterotaxy syndrome
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Unravelling the complexity of heterotaxy syndrome

BMJ case reports, 2023-10, Vol.16 (10), p.e256198 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-256198

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11
Bivalvular infective endocarditis complicated by perivalvular abscess and aorto-right atrium fistula
Bivalvular infective endocarditis complicated by perivalvular abscess and aorto-right atrium fistula
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Bivalvular infective endocarditis complicated by perivalvular abscess and aorto-right atrium fistula

BMJ case reports, 2023-10, Vol.16 (10), p.e255993 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-255993

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12
Parkes Weber syndrome: a rare cause of foot drop
Parkes Weber syndrome: a rare cause of foot drop
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Parkes Weber syndrome: a rare cause of foot drop

BMJ case reports, 2023-10, Vol.16 (10), p.e254455 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-254455

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13
Congenital colonic stenosis: an unusual cause of colonic obstruction masquerading as Hirschsprung’s disease in infancy
Congenital colonic stenosis: an unusual cause of colonic obstruction masquerading as Hirschsprung’s disease in infancy
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Congenital colonic stenosis: an unusual cause of colonic obstruction masquerading as Hirschsprung’s disease in infancy

BMJ case reports, 2023-09, Vol.16 (9), p.e255898 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-255898

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14
Congenital hypothyroidism: clinical examination relevance
Congenital hypothyroidism: clinical examination relevance
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Congenital hypothyroidism: clinical examination relevance

BMJ case reports, 2023-09, Vol.16 (9), p.e256718 [Peer Reviewed Journal]

2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-256718

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15
Neurological Waardenburg-Shah syndrome: a diagnostic challenge in a child with skin hypopigmentation and neurological manifestation
Neurological Waardenburg-Shah syndrome: a diagnostic challenge in a child with skin hypopigmentation and neurological manifestation
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Neurological Waardenburg-Shah syndrome: a diagnostic challenge in a child with skin hypopigmentation and neurological manifestation

BMJ case reports, 2022-06, Vol.15 (6), p.e250360 [Peer Reviewed Journal]

2022 BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-250360

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16
Non-surgical treatment of Lutembacher syndrome: combined percutaneous transcatheter therapy
Non-surgical treatment of Lutembacher syndrome: combined percutaneous transcatheter therapy
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Non-surgical treatment of Lutembacher syndrome: combined percutaneous transcatheter therapy

BMJ case reports, 2022-05, Vol.15 (5), p.e247984 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2021-247984 ;PMID: 35584855

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17
Falsely low glycosylated haemoglobin levels probably secondary to hypersplenism in a patient with diabetes mellitus
Falsely low glycosylated haemoglobin levels probably secondary to hypersplenism in a patient with diabetes mellitus
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Falsely low glycosylated haemoglobin levels probably secondary to hypersplenism in a patient with diabetes mellitus

BMJ case reports, 2024-04, Vol.17 (4), p.e260249 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2024-260249 ;PMID: 38575331

Digital Resources/Online E-Resources

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18
PYROXD1 -associated myopathy
PYROXD1 -associated myopathy
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PYROXD1 -associated myopathy

BMJ case reports, 2024-03, Vol.17 (3), p.e259907 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2024-259907 ;PMID: 38553017

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19
Autosomal recessive ALOX12B gene and consecutive collodion baby
Autosomal recessive ALOX12B gene and consecutive collodion baby
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Article 		Add to My Research

Autosomal recessive ALOX12B gene and consecutive collodion baby

BMJ case reports, 2024-03, Vol.17 (3), p.e257608 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-257608 ;PMID: 38514164

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20
Klippel-Trenaunay syndrome or not? An exploration of atypical presentations
Klippel-Trenaunay syndrome or not? An exploration of atypical presentations
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Klippel-Trenaunay syndrome or not? An exploration of atypical presentations

BMJ case reports, 2024-03, Vol.17 (3), p.e259763 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2024-259763 ;PMID: 38471707

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