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/vufind/Search/Results?lookfor=%22Pearson+syndrome%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22Pearson+syndrome%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
Search /vufind/Search2/Results?lookfor=%22Pearson+syndrome%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
PubPharm (65)
1
Atypical presentation of Pearson syndrome in an infant with suspected myelodysplastic syndrome
enthalten in:
Pediatric nephrology (Berlin, Germany)
| 2024
von
Tajan, A.
|
Riebel, A.
|
Zavala, M.
| +5
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2
Conduction defects in pediatric patients with Pearson syndrome : When to pace?
enthalten in:
Heart rhythm
| 2023
von
Shahid, S.
|
El Assaad, I.
|
Patel, A.
| +2
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3
Understanding the impact of pediatric single large-scale mtDNA deletion syndromes on caregivers : Burdens and challenges
enthalten in:
JIMD reports
| 2023
von
Chappell, M.
|
Parikh, S.
|
Reynolds, E.
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4
Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model
enthalten in:
Pharmacological research
| 2022
von
Ishikawa, K.
|
Honma, Y.
|
Yoshimi, A.
| +4
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5
Pearson syndrome : a multisystem mitochondrial disease with bone marrow failure
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Yoshimi, A.
|
Ishikawa, K.
|
Niemeyer, C.
| +1
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6
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Yoshimi, A.
|
Ishikawa, K.
|
Niemeyer, C.
| +1
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7
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Yoshimi, A.
|
Ishikawa, K.
|
Niemeyer, C.
| +1
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8
Development and characterization of cell models harbouring mtDNA deletions for in vitro study of Pearson syndrome
enthalten in:
Disease models & mechanisms
| 2022
von
Hernández-Ainsa, C.
|
López-Gallardo, E.
|
García-Jiménez, M.
| +7
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9
Extremely Rare Case of Fetal Anemia Due to Mitochondrial Disease Managed with Intrauterine Transfusion
enthalten in:
Medicina (Kaunas, Lithuania)
| 2022
von
Chung, J.
|
Lee, M.
|
Chung, J.
| +1
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10
Congenital etiologies of exocrine pancreatic insufficiency
enthalten in:
Frontiers in pediatrics
| 2022
von
Scheers, I.
|
Berardis, S.
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Journal of inherited metabolic disease
4
European journal of pediatrics
4
Indian journal of pediatrics
3
ClinicalTrials.gov
3
Journal of neurology
3
Orphanet journal of rare diseases
3
Pediatric blood & cancer
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American journal of medical genetics. Part A
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Archivos argentinos de pediatria
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Annals of noninvasive electrocardiology : the o...
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British journal of haematology
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Dubai Medical Journal
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Expert review of hematology
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Thema
41
Pearson syndrome
23
Journal Article
17
Pearson Syndrome
12
Case Reports
10
DNA, Mitochondrial
8
mtDNA
7
Research Support, Non-U.S. Gov't
5
Acyl-CoA Dehydrogenase, Long-Chain
5
EC 1.3.8.8
5
Kearns-Sayre syndrome
5
Review
4
Barth Syndrome
4
Failure to thrive
4
Hypoparathyroidism
4
Mitochondrial DNA deletion
4
Mitochondrial disorders
4
Mitochondrial genome
4
Natural history
4
Sideroblastic anemia
4
anemia
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Erscheinungszeitraum
61
2000-
4
1900-1999
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Sprache
64
Englisch
1
Spanisch
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