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Refined by: Journal Title: Bmj Case Reports remove subject: Humans remove subject: Infant, Newborn remove
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1
Congenital cerebriform plaque in a newborn
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Article
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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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2
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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3
Aplasia cutis congenita type VII of the lower extremity: a favourable disease course with minimal conservative treatment
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Aplasia cutis congenita type VII of the lower extremity: a favourable disease course with minimal conservative treatment

BMJ case reports, 2024-04, Vol.17 (4), p.e257572 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 BMJ Publishing Group Limited 2024. 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. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-257572 ;PMID: 38631814

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4
Alarming medication error with prostaglandin E1 (PGE1) in a term neonate with critical congenital heart disease
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Article
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Alarming medication error with prostaglandin E1 (PGE1) in a term neonate with critical congenital heart disease

BMJ case reports, 2024-04, Vol.17 (4), p.e259287 [Peer Reviewed Journal]

2024 BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-259287 ;PMID: 38589246

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5
Neonatal Bacillus cereus : an unusual case of congenital pneumonia requiring ECMO
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Article
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Neonatal Bacillus cereus : an unusual case of congenital pneumonia requiring ECMO

BMJ case reports, 2024-04, Vol.17 (4), p.e257965 [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-2023-257965 ;PMID: 38575335

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6
Simpson-Golabi-Behmel syndrome type 1 with normal birth parameters
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Article
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Simpson-Golabi-Behmel syndrome type 1 with normal birth parameters

BMJ case reports, 2024-03, Vol.17 (3), p.e247864 [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-2021-247864 ;PMID: 38442972

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7
Harlequin ichthyosis, prenatal diagnosis: the ultrasound recognition
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Article
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Harlequin ichthyosis, prenatal diagnosis: the ultrasound recognition

BMJ case reports, 2024-01, Vol.17 (1), p.e256859 [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. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-256859 ;PMID: 38233004

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8
Hydrometrocolpos: antenatal diagnosis and postnatal management
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Article
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Hydrometrocolpos: antenatal diagnosis and postnatal management

BMJ case reports, 2023-12, Vol.16 (12), p.e253985 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;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-2022-253985 ;PMID: 38129091

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9
Xanthogranulomatous pyelonephritis in neonate: presentation, management and outcome
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Article
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Xanthogranulomatous pyelonephritis in neonate: presentation, management and outcome

BMJ case reports, 2023-11, Vol.16 (11), p.e255258 [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-2023-255258 ;PMID: 38011955

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10
Congenital glottic stenosis as a clinical manifestation of FREM1 -associated disorders in a neonate with respiratory distress and aphonia
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Article
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Congenital glottic stenosis as a clinical manifestation of FREM1 -associated disorders in a neonate with respiratory distress and aphonia

BMJ case reports, 2024-05, Vol.17 (5), p.e257133 [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-2023-257133 ;PMID: 38719265

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11
Empirical overview of a delayed diagnosis of bilateral congenital choanal atresia in an adolescent male: management with 'coblation-assisted surgery'
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Article
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Empirical overview of a delayed diagnosis of bilateral congenital choanal atresia in an adolescent male: management with 'coblation-assisted surgery'

BMJ case reports, 2023-07, Vol.16 (7), p.e254865 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;2023 BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-254865 ;PMID: 37491123

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12
Osteogenesis imperfecta type VIII: highlighting the need for genetic testing
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Article
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Osteogenesis imperfecta type VIII: highlighting the need for genetic testing

BMJ case reports, 2023-07, Vol.16 (7), p.e253155 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;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. ;BMJ Publishing Group Limited 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2023 ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-253155 ;PMID: 37437959

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13
Aorta to left ventricle tunnel presenting with cardiac failure in a neonate
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Article
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Aorta to left ventricle tunnel presenting with cardiac failure in a neonate

BMJ case reports, 2024-01, Vol.17 (1), p.e255497 [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. ;ISSN: 1757-790X ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2023-255497 ;PMID: 38216156

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14
Primary congenital hypothyroidism: challenges in a low-income country without paediatric endocrinologist and universal newborn screening
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Article
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Primary congenital hypothyroidism: challenges in a low-income country without paediatric endocrinologist and universal newborn screening

BMJ case reports, 2023-05, Vol.16 (5), p.e249997 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;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-2022-249997 ;PMID: 37137550

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15
Vaginal bleeding in a newborn as initial presentation of uterus didelphys
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Article
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Vaginal bleeding in a newborn as initial presentation of uterus didelphys

BMJ case reports, 2023-02, Vol.16 (2), p.e251017 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;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-2022-251017 ;PMID: 36750302

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16
Acute aortic thrombosis following umbilical artery catheterisation in extremely low birthweight infants: walking the tight rope of management
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Article
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Acute aortic thrombosis following umbilical artery catheterisation in extremely low birthweight infants: walking the tight rope of management

BMJ case reports, 2023-11, Vol.16 (11), p.e256902 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;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-2023-256902 ;PMID: 37993142

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17
Novel mutation causing Zellweger syndrome
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Article
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Novel mutation causing Zellweger syndrome

BMJ case reports, 2023-03, Vol.16 (3), p.e252014 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;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-2022-252014 ;PMID: 36931687

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18
Rare cause of persistent hypocalcaemia in infancy due to PTH gene mutation
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Article
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Rare cause of persistent hypocalcaemia in infancy due to PTH gene mutation

BMJ case reports, 2023-09, Vol.16 (9), p.e256358 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;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-2023-256358 ;PMID: 37699739

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19
Response to sirolimus in a case of diffuse congenital hyperinsulinaemic hypoglycaemia due to homozygous KCNJ11 mutation
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Article
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Response to sirolimus in a case of diffuse congenital hyperinsulinaemic hypoglycaemia due to homozygous KCNJ11 mutation

BMJ case reports, 2022-11, Vol.15 (11), p.e252708 [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-2022-252708 ;PMID: 36410788

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20
Nodular lesions in a newborn: what is the diagnosis?
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Article
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Nodular lesions in a newborn: what is the diagnosis?

BMJ case reports, 2022-11, Vol.15 (11), p.e252229 [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-2022-252229 ;PMID: 36396329

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