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/vufind/Search/Results?lookfor=%22Sait%2C+Haseena%22&type=Person&sort=year
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PubPharm (37)
1
Inborn Errors of Ketogenesis : Novel Variants, Clinical Presentation, and Follow-Up in a Series of Four Patients
enthalten in:
Journal of pediatric genetics
| 2024
von
Sait, H.
|
Srivastava, S.
|
Kumar, S.
| +7
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2
Neurodegeneration with brain iron accumulation : a case series highlighting phenotypic and genotypic diversity in 20 Indian families
enthalten in:
Neurogenetics
| 2023
von
Sait, H.
|
Srivastava, S.
|
Pandey, M.
| +10
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3
T2 olivary nuclei hyperintensities : A characteristic neuroimaging finding in FIG4-related leukoencephalopathy
enthalten in:
American journal of medical genetics. Part A
| 2023
von
Sait, H.
|
Shambhavi, A.
|
Pandey, M.
| +2
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4
Anastrozole-mediated modulation of mitochondrial activity by inhibition of mitochondrial permeability transition pore opening : an initial perspective
enthalten in:
Journal of biomolecular structure & dynamics
| 2023
von
Kumar, S.
|
Choudhary, N.
|
Faruq, M.
| +14
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5
T2 olivary nuclei hyperintensities : A characteristic neuroimaging finding in FIG4‐related leukoencephalopathy
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2023
von
Sait, H.
|
Shambhavi, A.
|
Pandey, M.
| +2
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6
Autosomal recessive spinocerebellar ataxia-20 due to a novel SNX14 variant in an Indian girl
enthalten in:
American journal of medical genetics. Part A
| 2022
von
Sait, H.
|
Moirangthem, A.
|
Agrawal, V.
| +1
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7
Deciphering the molecular landscape of microcephaly in 87 Indian families by exome sequencing
enthalten in:
European journal of medical genetics
| 2022
von
Masih, S.
|
Moirangthem, A.
|
Shambhavi, A.
| +8
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8
Haemophilia management programme : Transformation during COVID-19
enthalten in:
The Indian journal of medical research
| 2022
von
Sait, H.
|
Sajjan, S.
|
Phadke, S.
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9
Congenital Hyperinsulinemia of Infancy : Role of Molecular Testing in Management and Genetic Counseling
enthalten in:
Indian journal of pediatrics
| 2022
von
Sait, H.
|
Sharma, L.
|
Dabadghao, P.
| +1
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10
Congenital Hyperinsulinemia of Infancy: Role of Molecular Testing in Management and Genetic Counseling
enthalten in:
Indian journal of pediatrics
| 2022
von
Sait, H.
|
Sharma, L.
|
Dabadghao, P.
| +1
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37
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Indian journal of pediatrics
6
Indian pediatrics
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American Journal of Medical Genetics Part C: Se...
2
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2
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1
Indian journal of dermatology
1
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1
bioRxiv.org
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Thema
12
Journal Article
6
Case Reports
4
Basal ganglia calcification
4
IgA nephropathy
4
Research Support, Non-U.S. Gov't
4
Skeletal dysplasia
4
Spondyloenchondrodysplasia with immune dysregul...
4
Systemic lupus erythematous
4
Type-1 interferonopathies
3
Congenital hyperinsulinemia
3
Loss of heterozygosity
3
Preconceptional counselling
3
Refractory hypoglycaemia
2
9002-71-5
2
Editorial
2
Letter
2
Newborn screening
2
Postpartum
2
Povidone iodine
2
Pregnant
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Erscheinungszeitraum
30
2020-
7
2010-2019
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Sprache
35
Englisch
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