skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 426  for All Library Resources

Results 1 2 3 4 5 next page
Show only
Refined by: Database: MEDLINE remove xxx: xxx remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report
Material Type:
Article
Add to My Research

Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report

Medicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Peer Reviewed Journal]

Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000031443 ;PMID: 36316845

Full text available

2
Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman
Material Type:
Article
Add to My Research

Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman

Internal Medicine, 2014, Vol.53(7), pp.783-787 [Peer Reviewed Journal]

2014 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.53.1325 ;PMID: 24694497

Full text available

3
Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX Mosaicism
Material Type:
Article
Add to My Research

Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX Mosaicism

Internal Medicine, 2009, Vol.48(6), pp.447-453 [Peer Reviewed Journal]

2009 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.48.1157 ;PMID: 19293545

Full text available

4
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
Material Type:
Article
Add to My Research

Doctors’ experiences of adverse events in secondary care: the professional and personal impact

Clinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Peer Reviewed Journal]

2014 © 2014 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;2015 INIST-CNRS ;2014 Royal College of Physicians 2014 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.14-6-585 ;PMID: 25468840

Full text available

5
Neurofibromatosis complicated with XXX syndrome and renovascular hypertension
Material Type:
Article
Add to My Research

Neurofibromatosis complicated with XXX syndrome and renovascular hypertension

Journal of internal medicine, 1996-06, Vol.239 (6), p.531-535 [Peer Reviewed Journal]

Blackwell Science Ltd ;1996 INIST-CNRS ;ISSN: 0954-6820 ;EISSN: 1365-2796 ;DOI: 10.1046/j.1365-2796.1996.422778000.x ;PMID: 8656147

Full text available

6
XXX 18-TRISOMY
Material Type:
Article
Add to My Research

XXX 18-TRISOMY

The Lancet (British edition), 1963-12, Vol.2 (7320), p.1276-1277 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 14066862

Full text available

7
Is the effect of melatonin on vascular endothelial growth factor receptor-2 associated with angiogenesis in the rat ovary?
Material Type:
Article
Add to My Research

Is the effect of melatonin on vascular endothelial growth factor receptor-2 associated with angiogenesis in the rat ovary?

Clinics (São Paulo, Brazil), 2019-01, Vol.74, p.e658-e658, Article e658 [Peer Reviewed Journal]

2019 CLINICS ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1807-5932 ;ISSN: 1980-5322 ;EISSN: 1980-5322 ;DOI: 10.6061/clinics/2019/e658 ;PMID: 30864638

Full text available

8
XXX 21-trisomy and retinoblastoma
Material Type:
Article
Add to My Research

XXX 21-trisomy and retinoblastoma

The Lancet (British edition), 1963-07, Vol.2 (7299), p.154-155 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 14025631

Full text available

9
Antenatal diagnosis of an XXX female. A dilemma for genetic counseling
Material Type:
Article
Add to My Research

Antenatal diagnosis of an XXX female. A dilemma for genetic counseling

The Western journal of medicine, 1975-07, Vol.123 (1), p.17-21 [Peer Reviewed Journal]

ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778

Full text available

10
XXY son of a possibly XX-XXX mother
Material Type:
Article
Add to My Research

XXY son of a possibly XX-XXX mother

The Lancet (British edition), 1972-03, Vol.1 (7752), p.697-698 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4125211

Full text available

11
XXY son of XX-XXX mother
Material Type:
Article
Add to My Research

XXY son of XX-XXX mother

The Lancet (British edition), 1972-04, Vol.1 (7757), p.955-955 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4112113

Full text available

12
Plasma factor-VIII concentrations in XXX women
Material Type:
Article
Add to My Research

Plasma factor-VIII concentrations in XXX women

The Lancet (British edition), 1971-01, Vol.1 (7689), p.58-59 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4099216

Full text available

13
The XXX syndrome frequency among mental defectives and fertility
Material Type:
Article
Add to My Research

The XXX syndrome frequency among mental defectives and fertility

The Lancet (British edition), 1960-09, Vol.2 (7151), p.626-627 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 13701513

Full text available

14
XO-XX-XXX mosaicism with Turner stigmata
Material Type:
Article
Add to My Research

XO-XX-XXX mosaicism with Turner stigmata

The Lancet (British edition), 1967-06, Vol.1 (7501), p.1228-1229 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4165148

Full text available

15
Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report
Material Type:
Article
Add to My Research

Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report

Medicine (Baltimore), 2020-07, Vol.99 (29), p.e20848-e20848 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020848 ;PMID: 32702826

Full text available

16
Chromosomal abnormalities detected by karyotyping among patients with secondary amenorrhea: a retrospective study
Material Type:
Article
Add to My Research

Chromosomal abnormalities detected by karyotyping among patients with secondary amenorrhea: a retrospective study

São Paulo medical journal, 2023, Vol.141 (5), p.e2022426-e2022426 [Peer Reviewed Journal]

This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1516-3180 ;ISSN: 1806-9460 ;EISSN: 1806-9460 ;DOI: 10.1590/1516-3180.2022.0426.R1.14012023 ;PMID: 37042862

Full text available

17
Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China
Material Type:
Article
Add to My Research

Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China

Medicine (Baltimore), 2021-02, Vol.100 (6), p.e24740-e24740 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024740 ;PMID: 33578623

Full text available

18
Integrating network pharmacology and experimental verification to explore the mechanism of Tripterygium wilfordii in ankylosing spondylitis
Material Type:
Article
Add to My Research

Integrating network pharmacology and experimental verification to explore the mechanism of Tripterygium wilfordii in ankylosing spondylitis

Medicine (Baltimore), 2023-12, Vol.102 (50), p.e36580-e36580 [Peer Reviewed Journal]

Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. 2023 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000036580 ;PMID: 38115356

Full text available

19
Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective Disorders
Material Type:
Article
Add to My Research

Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective Disorders

EBioMedicine, 2015-08, Vol.2 (8), p.909-918 [Peer Reviewed Journal]

2015 The Authors ;2015 The Authors 2015 ;ISSN: 2352-3964 ;EISSN: 2352-3964 ;DOI: 10.1016/j.ebiom.2015.06.012 ;PMID: 26425698

Full text available

20
Breastfeeding in Spain and the factors related to its establishment and maintenance: LAyDI Study (PAPenRed)
Material Type:
Article
Add to My Research

Breastfeeding in Spain and the factors related to its establishment and maintenance: LAyDI Study (PAPenRed)

Atención primaria, 2024-01, Vol.56 (1), p.102772-102772 [Peer Reviewed Journal]

Copyright © 2023 The Authors. Publicado por Elsevier España, S.L.U. All rights reserved. ;EISSN: 1578-1275 ;DOI: 10.1016/j.aprim.2023.102772 ;PMID: 37741187

Full text available

Results 1 - 20 of 426  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (417)

Refine My Results

Creation Date 

From To
  1. Before 1972  (18)
  2. 1972 To 1991  (19)
  3. 1992 To 2002  (32)
  4. 2003 To 2013  (97)
  5. After 2013  (261)
  6. More options open sub menu

Resource Type 

  1. Articles  (425)
  2. magazinearticle  (1)
  3. More options open sub menu

Language 

  1. English  (423)
  2. Japanese  (27)
  3. Portuguese  (7)
  4. Spanish  (3)
  5. Chinese  (1)
  6. French  (1)
  7. More options open sub menu

Searching Remote Databases, Please Wait