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مکتبة رقمیه للعلوم الطبيه
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Results of search for 'au:"Balwani, M"'
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Authors
Balwani, M
Balwani, M R
Bawankule, C P
Brancaleoni, V
Cappellini, M D
Desnick, R J
Di Pierro, E
Fiorentino, V
Fustinoni, S
Grace, M
Granata, F
Graziadei, G
Gumber, M R
Kute, V B
Missineo, P
Naik, H
Pardo, S
Patel, H V
Shah, P R
Trivedi, H L
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Topics
Age of Onset
Alleles
Child, Preschool
Dihydrolipoamide Dehydrogenase
Erythrocytes
Exons
Female
Genes, X-Linked
Genetic Diseases, X-Linked
Genotype
Heterozygote
Humans
Jews
Male
Metabolism, Inborn Errors
Mutation
North America
Nuclear Proteins
Pedigree
diagnosis
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Languages
English
g d
Your search returned 5 results.
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1.
Biochemical and molecular diagnosis of lipoamide dehydrogenase deficiency in a North American Ashkenazi Jewish family.
[electronic resource]
by
Sansaricq, C
Pardo, S
Balwani, M
Grace, M
Raymond, K
Producer:
20061016
In:
Journal of inherited metabolic disease
vol. 29
Online resources:
Available from publisher's website
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2.
Methylene Blue Induced Methemoglobinemia with Acute Kidney Injury in a Glucose-6-Phosphate Dehydrogenase-deficient Patient.
[electronic resource]
by
Balwani, M R
Bawankule, C P
Ramteke, V
Tolani, P
Vakil, S
Yadav, R
Publication details:
Indian journal of nephrology
In:
Indian journal of nephrology
vol. 27
Online resources:
Available from publisher's website
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No items available.
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3.
C1q Nephropathy in a Patient of Neurofibromatosis Type 1: A Rare Case Report.
[electronic resource]
by
Varyani, U T
Shah, N M
Shah, P R
Kute, V B
Balwani, M R
Trivedi, H L
Publication details:
Indian journal of nephrology
In:
Indian journal of nephrology
vol. 29
Online resources:
Available from publisher's website
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4.
Meningioma in long-term survivor after renal transplantation.
[electronic resource]
by
Kute, V B
Patel, H V
Vanikar, A V
Shah, P R
Gumber, M R
Balwani, M R
Trivedi, H L
Producer:
20130919
In:
Indian journal of nephrology
vol. 23
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5.
X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyria.
[electronic resource]
by
Brancaleoni, V
Balwani, M
Granata, F
Graziadei, G
Missineo, P
Fiorentino, V
Fustinoni, S
Cappellini, M D
Naik, H
Desnick, R J
Di Pierro, E
Producer:
20161013
In:
Clinical genetics
vol. 89
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