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Practice guidelines for the diagnosis and management of microcytic anemias due to genetic disorders of iron metabolism or heme synthesis
Practice guidelines for the diagnosis and management of microcytic anemias due to genetic disorders of iron metabolism or heme synthesis
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Practice guidelines for the diagnosis and management of microcytic anemias due to genetic disorders of iron metabolism or heme synthesis

Blood, 2014-06, Vol.123 (25), p.3873-3886 [Peer Reviewed Journal]

2014 American Society of Hematology ;2014 by The American Society of Hematology. ;ISSN: 0006-4971 ;ISSN: 1528-0020 ;EISSN: 1528-0020 ;DOI: 10.1182/blood-2014-01-548776 ;PMID: 24665134

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2
Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6 -Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia
Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6 -Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia
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Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6 -Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia

International journal of molecular sciences, 2022-02, Vol.23 (3), p.1917 [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: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms23031917 ;PMID: 35163840

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3
IRIDA Phenotype in TMPRSS6 Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology
IRIDA Phenotype in TMPRSS6 Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology
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IRIDA Phenotype in TMPRSS6 Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology

Genes, 2022-07, Vol.13 (8), p.1309 [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: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes13081309 ;PMID: 35893046

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4
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): evaluation of a national guideline on management of neonatal catheter-related thrombosis
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): evaluation of a national guideline on management of neonatal catheter-related thrombosis
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NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): evaluation of a national guideline on management of neonatal catheter-related thrombosis

BMC pediatrics, 2018-02, Vol.18 (1), p.84-84, Article 84 [Peer Reviewed Journal]

COPYRIGHT 2018 BioMed Central Ltd. ;COPYRIGHT 2018 BioMed Central Ltd. ;The Author(s). 2018 ;ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-018-1000-7 ;PMID: 29475450

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5
Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis: a multicentre, randomised controlled trial (NeoPIns)
Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis: a multicentre, randomised controlled trial (NeoPIns)
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Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis: a multicentre, randomised controlled trial (NeoPIns)

The Lancet (British edition), 2017-08, Vol.390 (10097), p.871-881 [Peer Reviewed Journal]

2017 Elsevier Ltd ;Copyright © 2017 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited Aug 26, 2017 ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(17)31444-7 ;PMID: 28711318

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6
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study
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C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study

Clinical infectious diseases, 2021-07, Vol.73 (2), p.e383-e390 [Peer Reviewed Journal]

ISSN: 1058-4838 ;EISSN: 1537-6591 ;DOI: 10.1093/cid/ciaa876

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7
Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis
Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis
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Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis

Blood, 2018-09, Vol.132 (13), p.1455-1458 [Peer Reviewed Journal]

2018 American Society of Hematology ;2018 by The American Society of Hematology 2018 ;ISSN: 0006-4971 ;EISSN: 1528-0020 ;DOI: 10.1182/blood-2018-06-854711 ;PMID: 30111608

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8
IRIDA Phenotype in ITMPRSS6/I Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology
IRIDA Phenotype in ITMPRSS6/I Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology
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IRIDA Phenotype in ITMPRSS6/I Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology

Genes, 2022-07, Vol.13 (8) [Peer Reviewed Journal]

COPYRIGHT 2022 MDPI AG ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes13081309

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9
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study
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C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study

ISSN: 1058-4838 ;EISSN: 1537-6591 ;DOI: 10.5167/uzh-192744 ;DOI: 10.1093/cid/ciaa876

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10
Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defects
Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defects
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Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defects

ISSN: 0902-4441 ;EISSN: 1600-0609 ;DOI: 10.1111/ejh.12995

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11
Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis:a multicentre, randomised controlled trial (NeoPIns)
Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis:a multicentre, randomised controlled trial (NeoPIns)
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Article 		Add to My Research

Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis:a multicentre, randomised controlled trial (NeoPIns)

ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(17)31444-7

Full text available

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12
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): evaluation of a national guideline on management of neonatal catheter-related thrombosis
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): evaluation of a national guideline on management of neonatal catheter-related thrombosis
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Article 		Add to My Research

NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): evaluation of a national guideline on management of neonatal catheter-related thrombosis

info:eu-repo/semantics/OpenAccess ;ISSN: 1471-2431 ;EISSN: 1471-2431

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13
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT) : evaluation of a national guideline on management of neonatal catheter-related thrombosis
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT) : evaluation of a national guideline on management of neonatal catheter-related thrombosis
Material Type:
Article 		Add to My Research

NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT) : evaluation of a national guideline on management of neonatal catheter-related thrombosis

info:eu-repo/semantics/OpenAccess ;ISSN: 1471-2431 ;EISSN: 1471-2431

Full text available

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14
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): Evaluation of a national guideline on management of neonatal catheter-related thrombosis
NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): Evaluation of a national guideline on management of neonatal catheter-related thrombosis
Material Type:
Article 		Add to My Research

NEOnatal Central-venous Line Observational study on Thrombosis (NEOCLOT): Evaluation of a national guideline on management of neonatal catheter-related thrombosis

ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-018-1000-7

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15
Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory
Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory
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Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory

info:eu-repo/semantics/OpenAccess ;ISSN: 0361-8609 ;EISSN: 1096-8652

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16
Iron refractory iron deficiency anemia:a heterogeneous disease that is not always iron refractory
Iron refractory iron deficiency anemia:a heterogeneous disease that is not always iron refractory
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Iron refractory iron deficiency anemia:a heterogeneous disease that is not always iron refractory

ISSN: 0361-8609 ;EISSN: 1096-8652 ;DOI: 10.1002/ajh.24561

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17
Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory
Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory
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Article 		Add to My Research

Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory

American Journal of Hematology, 2016-12, Vol.91 (12), p.E482-E490 [Peer Reviewed Journal]

ISSN: 0361-8609 ;EISSN: 1096-8652

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18
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study
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Article 		Add to My Research

C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study

DOI: 10.5281/zenodo.4719706

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19
Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis
Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis
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Reports 		Add to My Research

Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis

Blood, 2018, Vol.132 (13), p.1455-1458

EISSN: 1528-0020 ;DOI: 10.1182/blood-2018-06-854711

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