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Ziad Albahri

Observed names: Albahri Z, Albahri Ziad, Z. Albahri
OpenAlex ID: A5026717806
Screening and diagnosis of congenital disorders of glycosylation
2007 · Eliška Marklová, Ziad Albahri · Clinica Chimica Acta · 92
Genetic variants of transferrin in the diagnosis of protein hypoglycosylation
2005 · Z. Albahri, E. Marklová, et al. · Journal of Inherited Metabolic Disease · 16
Microheterogeneity of some serum glycoproteins in neurodegenerative diseases
2011 · Eliška Marklová, Ziad Albahri, et al. · Journal of the Neurological Sciences · 9
Our Experience with Diagnostics of Congenital Disorders of Glycosylation
2004 · Ziad Albahri, Eliška Marklová, et al. · Acta Medica (Hradec Kralove Czech Republic) · 8
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Churg-Strauss Syndrome in Childhood
2013 · Ziad Albahri, Lenka Minxová, et al. · Journal of Child Neurology · 7
Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG)
2009 · Eliška Marklová, Ziad Albahri · Journal of Clinical Laboratory Analysis · 7
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Pitfalls and drawbacks in screening of congenital disorders of glycosylation
2004 · Eliška Marklová, Ziad Albahri · Clinical Chemistry and Laboratory Medicine (CCLM) · 7
Congenital Disorders of Glycosylation: A Review
2015 · Ziad Albahri · Asian Journal of Psychiatry · 5
Development of Pulmonary Hypertension in an Infant Treated With Diazoxide for Hyperinsulinism, a Case Report and Literature Review
2015 · Ziad Albahri, Antonín Lukeš, et al. · Asian Journal of Psychiatry · 5
Difuse Infantile Hemangiomatosis with Consumptive Hypothyroidism in an Infant: A Case Report
2016 · Ziad Albahri · American Journal of Pediatrics · 4
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Genetic variants of transferrin in cystic fibrosis
2008 · E. Marklová, Z. Albahri, et al. · Journal of Inherited Metabolic Disease · 4
Mortality benefit of primary transportation to a PCI‐capable center persists through an eight‐year follow‐up in patients with ST‐segment elevation myocardial infarction
2017 · Abdulwasya Almawiri, Vojacek Jan, et al. · Journal of Interventional Cardiology · 3
Amniotic fluid α-fetoprotein microheterogeneity in the prenatal diagnosis of congenital disorders of glycosylation type Ia
2010 · Eliška Marklová, Ziad Albahri · Clinical Chemistry and Laboratory Medicine (CCLM) · 3
CDG: a new case of a combined defect in the biosynthesis of N- and O-glycans
2006 · Ziad Albahri, Eliška Marklová, et al. · European Journal of Pediatrics · 2
Peripheral facial paralysis in an infant with malignant hypertension and suspected neurofibromatosis disease
2015 · Z. Albahri, A. Lukeš, et al. · Journal of the Neurological Sciences · 1
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HPLC Profiling of Trp-related Metabolites In Humans
2003 · Eliška Marklová, Ziad Albahri, et al. · Advances in experimental medicine and biology · 1
Primary versus secondary transport in patients with acute ST-segment elevation myocardial infarction, times and mortality rates
2017 · Abdul Almawiri, Jan F. Vojáček, et al. · Intervenční a akutní kardiologie
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Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report
2015 · Ziad Albahri, Kateřina Krylová, et al. · Asian Journal of Psychiatry
Scalp Defect (Giant Aplasia Cutis Congenita of the Scalp in a Newborn)
2015 · Albahri Z, Krylova K, et al. · Pediatric Oncall
Peripheral neuropathies in childhood, a case report of Churg–/INS;Strauss syndrome in a Czech patient
2013 · Z. Albahri, L. Minxová, et al. · Journal of the Neurological Sciences
A case of infant with ischemic stroke after varicella infection
2013 · Z. Albahri, L. Minxová, et al. · Journal of the Neurological Sciences
Hypoglycosylation and disease modifying polymorphism in cystic fibrosis
2008 · E. Marklova, Z. Albahri, et al. · Journal of Cystic Fibrosis
Screening of congenital disorders of glycosylation
2006 · Ziad Albahri · Digital Repository (National Repository of Grey Literature)
Works count: 23
Citation count: 174
H-index: 7
I10-index: 2
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