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PubPharm (270)
1
Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Altassan, R.
|
AlQudairy, H.
|
AlJebreen, S.
| +10
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2
Novel UBE3B mutations : report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population
enthalten in:
Clinical dysmorphology
| 2024
von
Albakheet, A.
|
Almuallami, D.
|
Almass, R.
| +10
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3
Schizophrenia endothelial cells exhibit higher permeability and altered angiogenesis patterns in patient-derived organoids
enthalten in:
Translational psychiatry
| 2024
von
Stankovic, I.
|
Notaras, M.
|
Wolujewicz, P.
| +4
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4
Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2024
von
Altassan, R.
|
AlQudairy, H.
|
AlJebreen, S.
| +10
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5
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
enthalten in:
Acta neuropathologica
| 2023
von
Deng, R.
|
Medico-Salsench, E.
|
Nikoncuk, A.
| +49
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6
Investigation of Ganciclovir Resistance in Cytomegalovirus Isolates by Phenotypic and Genotypic Methods
enthalten in:
Mikrobiyoloji bulteni
| 2023
von
Sarınoğlu, R.
|
Çolak, D.
|
Küpesiz, O.
| +9
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7
Exposure to Cadmium Telluride Quantum Dots and Gene Expression Profile of Huh-7 Hepatocellular Carcinoma Cell Line
enthalten in:
Dose-response : a publication of International Hormesis Society
| 2023
von
Alothaid, H.
|
Al-Anazi, M.
|
Al-Qahtani, A.
| +8
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8
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
enthalten in:
Acta neuropathologica
| 2023
von
Deng, R.
|
Medico-Salsench, E.
|
Nikoncuk, A.
| +49
Wird geladen...
9
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
enthalten in:
Acta neuropathologica
| 2023
von
Deng, R.
|
Medico-Salsench, E.
|
Nikoncuk, A.
| +49
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10
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
enthalten in:
Acta neuropathologica
| 2023
von
Deng, R.
|
Medico-Salsench, E.
|
Nikoncuk, A.
| +49
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