Suchergebnisse - "Yamamoto, Raina"

PubPharm (23)

1

Luspatercept, a two-edged sword in beta-thalassemia-associated paravertebral extramedullary hematopoietic masses (EHMs)

enthalten in: European journal of haematology | 2022

von Alashkar, F. | Klump, H. | Lange, C. | +8

2

Screening and diagnosis of hemoglobinopathies in Germany : Current state and future perspectives

enthalten in: Scientific reports | 2022

von Aramayo-Singelmann, C. | Halimeh, S. | Proske, P. | +8

3

Luspatercept, a two‐edged sword in beta‐thalassemia‐associated paravertebral extramedullary hematopoietic masses (EHMs)

enthalten in: European Journal of Haematology | 2022

von Alashkar, F. | Klump, H. | Lange, C. | +8

4

Pregnancies and Neonatal Outcomes in Patients with Sickle Cell Disease (SCD) : Still a (High-)Risk Constellation?

enthalten in: Journal of personalized medicine | 2021

von Proske, P. | Distelmaier, L. | Aramayo-Singelmann, C. | +14

5

Succinyl-CoA:3-oxoacid coenzyme a transferase (SCOT) deficiency : a rare and potentially fatal metabolic disease

enthalten in: Biochimie | 14 February 2021

von Grünert, S. | Foster, W. | Schumann, A. | +15

6

Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency : A rare and potentially fatal metabolic disease

enthalten in: Biochimie | 2021

von Grünert, S. | Foster, W. | Schumann, A. | +15

7

Laboratory reporting on the clinical spectrum of CFTR p.Arg117His : Still room for improvement

enthalten in: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2020

von Laudus, N. | Audrézet, M. | Girodon, E. | +8

8

A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family

enthalten in: Neurobiology of aging | 2020

von Mengel, D. | Liu, L. | Yamamoto, R. | +6

9

Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3 : a case report and review of literature

enthalten in: BMC endocrine disorders | 2019

von Joseph, A. | Sirisena, N. | Kumanan, T. | +5

10

Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature

enthalten in: BMC endocrine disorders | 2019

von Joseph, A. | Sirisena, N. | Kumanan, T. | +5