Suchergebnisse

PubPharm (259)

1

Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients

enthalten in: Genes | 2024

von Ivantsik, O. | John, A. | Kydonopoulou, K. | +4

2

Genetic Counseling and Genetic Testing for Familial Hypercholesterolemia

enthalten in: Genes | 2024

von Tada, H. | Kawashiri, M. | Nohara, A. | +3

3

Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision Medicine

enthalten in: Genes | 2024

von Snyder, H. | Jain, P. | RamachandranNair, R. | +2

4

Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs

enthalten in: Genes | 2024

von Freyer, J. | Labadie, J. | Huff, J. | +4

5

Hearing Loss : Genetic Testing, Current Advances and the Situation in Latin America

enthalten in: Genes | 2024

von De Rosa, M. | Bernardi, M. | Kleppe, S. | +1

6

Leptin and Leptin Receptor Polymorphisms in Infants and Their Parents : Correlation with Preterm Birth

enthalten in: Genes | 2024

von Savino, F. | Sardo, A. | Gambarino, S. | +5

7

Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients

in: Genes | 2024

von Ouliana Ivantsik | Anne John | Kyriaki Kydonopoulou | +4

8

Genetic Counseling and Genetic Testing for Familial Hypercholesterolemia

in: Genes | 2024

von Hayato Tada | Masa-aki Kawashiri | Atsushi Nohara | +3

9

Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision Medicine

in: Genes | 2024

von Hannah E. Snyder | Puneet Jain | Rajesh RamachandranNair | +2

10

DNAJB11 Mutation in ADPKD Patients : Clinical Characteristics in a Monocentric Cohort

enthalten in: Genes | 2023

von Aiello, V. | Ciurli, F. | Conti, A. | +13

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