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21
100 consecutive minimally invasive Heller myotomies: Lessons learned. Discussion
100 consecutive minimally invasive Heller myotomies: Lessons learned. Discussion
Material Type:
Conference Proceeding 		Add to My Research

100 consecutive minimally invasive Heller myotomies: Lessons learned. Discussion

Annals of surgery, 2002, Vol.235 (5), p.631-639 [Peer Reviewed Journal]

2002 INIST-CNRS ;ISSN: 0003-4932 ;EISSN: 1528-1140 ;CODEN: ANSUA5

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22
100 days outcome of severe wasting in hospitalised infants <6 months of age
100 days outcome of severe wasting in hospitalised infants <6 months of age
Material Type:
Article 		Add to My Research

100 days outcome of severe wasting in hospitalised infants <6 months of age

Public health nutrition, 2021-12, Vol.24 (17), p.5847-5856 [Peer Reviewed Journal]

The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society ;The Authors 2021 2021 The Authors ;ISSN: 1368-9800 ;EISSN: 1475-2727 ;DOI: 10.1017/S1368980021003268 ;PMID: 34353402

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23
1,000 consecutive children with a cardiac malformation with 26- to 37-year follow-up
1,000 consecutive children with a cardiac malformation with 26- to 37-year follow-up
Material Type:
Article 		Add to My Research

1,000 consecutive children with a cardiac malformation with 26- to 37-year follow-up

The American journal of cardiology, 1992-09, Vol.70 (6), p.661-667 [Peer Reviewed Journal]

1992 ;1993 INIST-CNRS ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/0002-9149(92)90209-H ;PMID: 1510017 ;CODEN: AJCDAG

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24
1000 Days: The "WeCare Generation" Program-The Ultimate Model for Improving Human Mental Health and Economics: The Study Protocol
1000 Days: The "WeCare Generation" Program-The Ultimate Model for Improving Human Mental Health and Economics: The Study Protocol
Material Type:
Article 		Add to My Research

1000 Days: The "WeCare Generation" Program-The Ultimate Model for Improving Human Mental Health and Economics: The Study Protocol

International journal of environmental research and public health, 2022-12, Vol.19 (24), p.16741 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph192416741 ;PMID: 36554625

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25
10,000 Anonymous Gift to Aid Sick Boy: Home Edition
10,000 Anonymous Gift to Aid Sick Boy: Home Edition
Material Type:
Newspaper Article 		Add to My Research

10,000 Anonymous Gift to Aid Sick Boy: Home Edition

The Los Angeles times, 1992-10-15

ISSN: 0458-3035 ;EISSN: 2165-1736

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26
10,000 ill children can shine in hospitals' poster contest: FIN Edition
10,000 ill children can shine in hospitals' poster contest: FIN Edition
Material Type:
Newspaper Article 		Add to My Research

10,000 ill children can shine in hospitals' poster contest: FIN Edition

Toronto star, 1988-05-13

Copyright 1988 Toronto Star, All Rights Reserved. ;ISSN: 0319-0781

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27
10,000 pregnant women, 5,000 new-born babies in 7 districts to be screened for genetic diseases
10,000 pregnant women, 5,000 new-born babies in 7 districts to be screened for genetic diseases
Material Type:
Newspaper Article 		Add to My Research

10,000 pregnant women, 5,000 new-born babies in 7 districts to be screened for genetic diseases

Businessline, 2019-09-25

Copyright THG Publishing Private Limited Sep 25, 2019

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28
1017 Unusual clinical course of congenital central hypoventilation syndrome: is outgrowing the syndrome possible?
1017 Unusual clinical course of congenital central hypoventilation syndrome: is outgrowing the syndrome possible?
Material Type:
Article 		Add to My Research

1017 Unusual clinical course of congenital central hypoventilation syndrome: is outgrowing the syndrome possible?

Sleep (New York, N.Y.), 2019-04, Vol.42 (Supplement_1), p.A409-A410 [Peer Reviewed Journal]

Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com. ;ISSN: 0161-8105 ;EISSN: 1550-9109 ;DOI: 10.1093/sleep/zsz069.1014

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29
104 Stereotactic Radiosurgery for Spetzler-Martin Grade IV and V Arteriovenous Malformations: An International Multicenter Study
104 Stereotactic Radiosurgery for Spetzler-Martin Grade IV and V Arteriovenous Malformations: An International Multicenter Study
Material Type:
Article 		Add to My Research

104 Stereotactic Radiosurgery for Spetzler-Martin Grade IV and V Arteriovenous Malformations: An International Multicenter Study

Neurosurgery, 2017-09, Vol.64 (CN_suppl_1), p.220-221 [Peer Reviewed Journal]

Copyright © 2017 by the Congress of Neurological Surgeons 2017 ;Copyright © by the Congress of Neurological Surgeons ;Copyright © 2017 Congress of Neurological Surgeons ;ISSN: 0148-396X ;EISSN: 1524-4040 ;DOI: 10.1093/neuros/nyx417.104

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30
105&#8197;ALG6-CDG- congenital disorder of glycosylation with recognizable phenotype
105&#8197;ALG6-CDG- congenital disorder of glycosylation with recognizable phenotype
Material Type:
Article 		Add to My Research

105 ALG6-CDG- congenital disorder of glycosylation with recognizable phenotype

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A44-A45 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2021-europaediatrics.105

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31
106: REVIEW OF SCREENING PROGRAM EFFECT ON INCIDENCE OF HEMOLYTIC DISEASE DUE TO G6PD DEFICIENCIES
106: REVIEW OF SCREENING PROGRAM EFFECT ON INCIDENCE OF HEMOLYTIC DISEASE DUE TO G6PD DEFICIENCIES
Material Type:
Article 		Add to My Research

106: REVIEW OF SCREENING PROGRAM EFFECT ON INCIDENCE OF HEMOLYTIC DISEASE DUE TO G6PD DEFICIENCIES

BMJ open, 2017-02, Vol.7 (Suppl 1), p.bmjopen-2016-015415.106 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2017 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. ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2017 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2016-015415.106

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32
1060 Novel Case of REM Behavior Disorder in a Pediatric PSG
1060 Novel Case of REM Behavior Disorder in a Pediatric PSG
Material Type:
Article 		Add to My Research

1060 Novel Case of REM Behavior Disorder in a Pediatric PSG

Sleep (New York, N.Y.), 2019-04, Vol.42 (Supplement_1), p.A425-A425 [Peer Reviewed Journal]

Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com. ;ISSN: 0161-8105 ;EISSN: 1550-9109 ;DOI: 10.1093/sleep/zsz069.1057

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33
108. ADDITIONAL PATHOGENIC IRF6 MUTATIONS IN VAN DER WOUDE SYNDROME FROM SUB-SAHARAN AFRICAN POPULATIONS
108. ADDITIONAL PATHOGENIC IRF6 MUTATIONS IN VAN DER WOUDE SYNDROME FROM SUB-SAHARAN AFRICAN POPULATIONS
Material Type:
Article 		Add to My Research

108. ADDITIONAL PATHOGENIC IRF6 MUTATIONS IN VAN DER WOUDE SYNDROME FROM SUB-SAHARAN AFRICAN POPULATIONS

The Cleft palate-craniofacial journal, 2016-07, Vol.53 (4), p.E127 [Peer Reviewed Journal]

Copyright Allen Press Publishing Services Jul 2016 ;ISSN: 1055-6656 ;EISSN: 1545-1569 ;CODEN: CPJOEG

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34
108 Andean bears, an endangered species, were analysed
108 Andean bears, an endangered species, were analysed
Material Type:
Newsletter Article 		Add to My Research

108 Andean bears, an endangered species, were analysed

CE Noticias Financieras, 2020

CE Noticias Financieras English, Latin America - Distributed by ContentEngine LLC

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35
108&#8197;Methylation biomarkers S-adenosylmethionine and S-adenosylhomocysteine and methylation potential in newborns with congenital heart disease and their mothers
108&#8197;Methylation biomarkers S-adenosylmethionine and S-adenosylhomocysteine and methylation potential in newborns with congenital heart disease and their mothers
Material Type:
Article 		Add to My Research

108 Methylation biomarkers S-adenosylmethionine and S-adenosylhomocysteine and methylation potential in newborns with congenital heart disease and their mothers

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A46-A46 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2021-europaediatrics.108

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36
10p Duplication characterized by fluorescence in situ hybridization
10p Duplication characterized by fluorescence in situ hybridization
Material Type:
Article 		Add to My Research

10p Duplication characterized by fluorescence in situ hybridization

American journal of medical genetics, 1994-09, Vol.52 (3), p.315-318 [Peer Reviewed Journal]

Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company ;1994 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320520312 ;PMID: 7528972 ;CODEN: AJMGDA

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37
10p12.1 deletion: HDR phenotype without DGS2 features
10p12.1 deletion: HDR phenotype without DGS2 features
Material Type:
Article 		Add to My Research

10p12.1 deletion: HDR phenotype without DGS2 features

Experimental and molecular pathology, 2009-02, Vol.86 (1), p.74-76 [Peer Reviewed Journal]

2008 Elsevier Inc. ;2009 INIST-CNRS ;ISSN: 0014-4800 ;EISSN: 1096-0945 ;DOI: 10.1016/j.yexmp.2008.10.003 ;PMID: 19022243 ;CODEN: EXMPA6

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38
1:1 atrioventricular conduction in congenital complete heart block
1:1 atrioventricular conduction in congenital complete heart block
Material Type:
Article 		Add to My Research

1:1 atrioventricular conduction in congenital complete heart block

Heart (British Cardiac Society), 1998-11, Vol.80 (5), p.525-526 [Peer Reviewed Journal]

British Cardiac Society ;1999 INIST-CNRS ;Copyright: 1998 British Cardiac Society ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/hrt.80.5.525 ;PMID: 9930058

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39
11-Keto-testosterone and other androgens of adrenal origin
11-Keto-testosterone and other androgens of adrenal origin
Material Type:
Article 		Add to My Research

11-Keto-testosterone and other androgens of adrenal origin

Physiological research, 2020-09, Vol.69 (Suppl 2), p.S187-S192 [Peer Reviewed Journal]

Copyright Institute of Physiology 2020 ;2020 Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic 2020 ;ISSN: 0862-8408 ;EISSN: 1802-9973 ;DOI: 10.33549/physiolres.934516 ;PMID: 33094617

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40
11-Month-Old Little brave heart Anjali gets a new lease of life at Medica Superspecialty Hospital
11-Month-Old Little brave heart Anjali gets a new lease of life at Medica Superspecialty Hospital
Material Type:
Newsletter Article 		Add to My Research

11-Month-Old Little brave heart Anjali gets a new lease of life at Medica Superspecialty Hospital

United News of India, 2021

Copyright HT Digital Streams Limited Jul 22, 2021

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