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1
Haddad syndrome: a case report
Haddad syndrome: a case report
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Haddad syndrome: a case report

Paediatrics and Family Medicine, 2021-01, Vol.17 (4), p.350-353 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2021.0056

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2
A review of practical issues related to the diseases of the nail unit useful for doctors (including non-dermatologists)
A review of practical issues related to the diseases of the nail unit useful for doctors (including non-dermatologists)
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A review of practical issues related to the diseases of the nail unit useful for doctors (including non-dermatologists)

Paediatrics and Family Medicine, 2020-01, Vol.16 (1), p.62-69 [Peer Reviewed Journal]

2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2020.0011

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3
Wrodzony kręcz szyi u niemowlęcia
Wrodzony kręcz szyi u niemowlęcia
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Wrodzony kręcz szyi u niemowlęcia

Paediatrics and Family Medicine, 2023-01, Vol.19 (2), p.131-134 [Peer Reviewed Journal]

Copyright Medical Communications Sp. z o.o. 2023 ;ISSN: 1734-1531 ;DOI: 10.15557/PÍMR.2023.0023

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4
Bell’s palsy or congenital cholesteatoma? A case report
Bell’s palsy or congenital cholesteatoma? A case report
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Bell’s palsy or congenital cholesteatoma? A case report

Paediatrics and Family Medicine, 2021-01, Vol.17 (3), p.284 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;DOI: 10.15557/PiMR.2021.0045

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5
Perinatal hypophosphatasia
Perinatal hypophosphatasia
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Perinatal hypophosphatasia

Paediatrics and Family Medicine, 2020-01, Vol.16 (3), p.306-311 [Peer Reviewed Journal]

2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2020.0056

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6
Adrenal crisis as a life-threatening condition
Adrenal crisis as a life-threatening condition
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Adrenal crisis as a life-threatening condition

Paediatrics and Family Medicine, 2021-01, Vol.17 (3), p.211-214 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2021.0032

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7
The development of the Sabin–Pinkerton triad despite prenatal screening for congenital toxoplasmosis
The development of the Sabin–Pinkerton triad despite prenatal screening for congenital toxoplasmosis
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The development of the Sabin–Pinkerton triad despite prenatal screening for congenital toxoplasmosis

Paediatrics and Family Medicine, 2021-01, Vol.17 (3), p.270-274 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2021.0042

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8
‘Unfortunate creatures’: The hazards of syphilis in wet-nursing
‘Unfortunate creatures’: The hazards of syphilis in wet-nursing
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‘Unfortunate creatures’: The hazards of syphilis in wet-nursing

Medycyna nowożytna : studia nad historią medycyny, 2020, Vol.26 (2), p.21-56 [Peer Reviewed Journal]

2020. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.ejournals.eu/MedycynaNowozytna/zakladka/917 ;ISSN: 1231-1960 ;EISSN: 2657-506X ;DOI: 10.4467/12311960MN.20.011.13353

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9
Laryngeal cleft type IV: a rare entity
Laryngeal cleft type IV: a rare entity
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Laryngeal cleft type IV: a rare entity

Paediatrics and Family Medicine, 2019-01, Vol.15 (1), p.81-84 [Peer Reviewed Journal]

2019. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2019.0014

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10
Isolated splenic vein thrombosis as a complication of abdominal trauma in a 3-month-old girl
Isolated splenic vein thrombosis as a complication of abdominal trauma in a 3-month-old girl
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Isolated splenic vein thrombosis as a complication of abdominal trauma in a 3-month-old girl

Paediatrics and Family Medicine, 2021-01, Vol.17 (3), p.275-278 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2021.0043

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11
Pfeiffer syndrome – a case report
Pfeiffer syndrome – a case report
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Article 		Add to My Research

Pfeiffer syndrome – a case report

Paediatrics and Family Medicine, 2021-01, Vol.17 (4), p.358-361 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2021.0058

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12
Hypothyroidism in children
Hypothyroidism in children
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Hypothyroidism in children

Paediatrics and Family Medicine, 2017-01, Vol.13 (4), p.479-490 [Peer Reviewed Journal]

2017. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2017.0051

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13
Multiple sclerosis and syringomyelia – a case report
Multiple sclerosis and syringomyelia – a case report
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Article 		Add to My Research

Multiple sclerosis and syringomyelia – a case report

Aktualności neurologiczne, 2019-01, Vol.19 (1), p.45-48 [Peer Reviewed Journal]

2019. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1641-9227 ;EISSN: 2451-0696 ;DOI: 10.15557/AN.2019.0008

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14
Early diagnosis of congenital vascular malformation as a condition to rapid prevention of complications – case study
Early diagnosis of congenital vascular malformation as a condition to rapid prevention of complications – case study
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Early diagnosis of congenital vascular malformation as a condition to rapid prevention of complications – case study

Paediatrics and Family Medicine, 2017-01, Vol.13 (2), p.260-266 [Peer Reviewed Journal]

2017. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2017.0028

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15
Wolf–Hirschhorn syndrome – a case report
Wolf–Hirschhorn syndrome – a case report
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Article 		Add to My Research

Wolf–Hirschhorn syndrome – a case report

Paediatrics and Family Medicine, 2017-06, Vol.13 (2), p.267-269 [Peer Reviewed Journal]

2017. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2017.0029

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16
Mowat–Wilson syndrome – case study
Mowat–Wilson syndrome – case study
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Article 		Add to My Research

Mowat–Wilson syndrome – case study

Paediatrics and Family Medicine, 2016-01, Vol.12 (2), p.201-208 [Peer Reviewed Journal]

2016. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;EISSN: 2451-0742 ;DOI: 10.15557/PiMR.2016.0020

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17
How to differentiate vomiting in neonates and infants? Part IV. Metabolic, endocrinologic and cardiovascular causes of vomiting
How to differentiate vomiting in neonates and infants? Part IV. Metabolic, endocrinologic and cardiovascular causes of vomiting
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Article 		Add to My Research

How to differentiate vomiting in neonates and infants? Part IV. Metabolic, endocrinologic and cardiovascular causes of vomiting

Paediatrics and Family Medicine, 2014-01, Vol.10 (1), p.50 [Peer Reviewed Journal]

2014. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;DOI: 10.15557/PiMR.2014.0007

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18
End-stage renal disease in the course of urinary tract defects in Wolf–Hirschhorn syndrome – case report
End-stage renal disease in the course of urinary tract defects in Wolf–Hirschhorn syndrome – case report
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End-stage renal disease in the course of urinary tract defects in Wolf–Hirschhorn syndrome – case report

Paediatrics and Family Medicine, , Vol.10 (3), p.322 [Peer Reviewed Journal]

2014. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531 ;DOI: 10.15557/PiMR.2014.0035

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19
Late recognition of genitourinary tract defect, such as doubling of vagina and uterus coexisted with right kidney agenesis – case presentation
Late recognition of genitourinary tract defect, such as doubling of vagina and uterus coexisted with right kidney agenesis – case presentation
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Article 		Add to My Research

Late recognition of genitourinary tract defect, such as doubling of vagina and uterus coexisted with right kidney agenesis – case presentation

Paediatrics and Family Medicine, 2008-01, Vol.4 (3), p.195 [Peer Reviewed Journal]

2008. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1734-1531

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