P. G. Barth - Publications, H-index & Citations

P. G. Barth

ruhr university bochum

72H指数

431论文数

1.6W被引数

收录论文 92

发表时间

Initial Results of 68Ga-FAPI-46 PET/MRI to Assess Response to Neoadjuvant Chemotherapy in Breast Cancer

JOURNAL OF NUCLEAR MEDICINE

IF9.1

2022-11-17

PREAI

Backhaus, Philipp; Burg, Matthias C.; Asmus, Inga; Pixberg, Michaela; Buethers, Florian; Breyholz, Hans-Joerg; Yeh, Randy; Weigel, Stefanie B.; Stichling, Patricia; Heindel, Walter; Bobe, Stefanie; Barth, Peter; Tio, Joke; Schaefers, Michael

Simultaneous FAPI PET/MRI Targeting the Fibroblast-Activation Protein for Breast Cancer

RADIOLOGY

IF15.2

2022-01-01

PREAI

Backhaus, Philipp; Burg, Matthias C.; Roll, Wolfgang; Buether, Florian; Breyholz, Hans-Joerg; Weigel, Stefanie; Heindel, Walter; Pixberg, Michaela; Barth, Peter; Tio, Joke; Schaefers, Michael

Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2019-11-07

OAAI

Mazar, Iyar; Stokes, Jonathan; Ollis, Sarah; Love, Emily; Espensen, Ashlee; Barth, Peter G.; Powers, John H., III; Shields, Alan L.

Validation and Reference Values for Three-Dimensional Echocardiographic Right Ventricular Volumetry in Children: A Multicenter Study

JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY

IF6

2018-09-01

PREAI

Laser, Kai Thorsten; Karabiyik, Ayse; Koerperich, Hermann; Horst, Jan-Pit; Barth, Peter; Kececioglu, Deniz; Burchert, Wolfgang; DallaPozza, Robert; Herberg, Ulrike

What's new in pontocerebellar hypoplasia? An update on genes and subtypes 什么是新的桥小脑发育不全？基因和亚型的最新进展

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2018-06-15

106

OAAI

van Dijk, Tessa; Baas, Frank; Barth, Peter G.; Poll-The, Bwee Tien

Pontocerebellar hypoplasia with spinal muscular atrophy (PCH1): identification of SLC25A46 mutations in the original Dutch PCH1 family

BRAIN

IF11.7

2017-06-20

OAAI

van Dijk, Tessa; Rudnik-Schoeneborn, Sabine; Senderek, Jan; Hajmousa, Ghazaleh; Mei, Hailiang; Dusl, Marina; Aronica, Eleonora; Barth, Peter; Baas, Frank

Deregulated expression of EZH2 in congenital brainstem disconnection

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

IF3.4

2017-05-22

OAAI

Barth, P. G.; Aronica, E.; Fox, S.; Fluiter, K.; Weterman, M. A. J.; Poretti, A.; Miller, D. C.; Boltshauser, E.; Harding, B.; Santi, M.; Baas, F.

TUBEROUS SCLEROSIS AND DYSPLASIA OF CORPUS-CALLOSUM - CASE-REPORT OF THEIR COMBINED OCCURRENCE IN A NEWBORN

ACTA NEUROPATHOLOGICA

IF9.3

2016-06-11

PREAI

BARTH, PG; STAM, FC; HARTEN, JJVD

Determination of 22 trace elements in high-purity copper including Se and Te by ETV-ICP OES using SF6, NF3, CF4 and H2 as chemical modifiers

JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY

IF3.1

2016-01-01

PREAI

Hassler, J.; Matschat, R.; Richter, S.; Barth, P.; Detcheva, A. K.; Waarto, H. -J.

Calculation of Pediatric Left Ventricular Mass: Validation and Reference Values Using Real-Time Three-Dimensional Echocardiography

JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY

IF6

2015-03-01

PREAI

Laser, Kai Thorsten; Houben, Britta Anna; Koerperich, Hermann; Haas, Nikolaus Alexander; Kelter-Kloepping, Andrea; Barth, Peter; Burchert, Wolfgang; DallaPozza, Robert; Kececioglu, Deniz; Herberg, Ulrike

Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies

HUMAN MUTATION

IF3.7

2014-11-24

108

OAAI

Lehtokari, Vilma-Lotta; Kiiski, Kirsi; Sandaradura, Sarah A.; Laporte, Jocelyn; Repo, Pauliina; Frey, Jennifer A.; Donner, Kati; Marttila, Minttu; Saunders, Carol; Barth, Peter G.; den Dunnen, Johan T.; Beggs, Alan H.; Clarke, Nigel F.; North, Kathryn N.; Laing, Nigel G.; Romero, Norma B.; Winder, Thomas L.; Pelin, Katarina; Wallgren-Pettersson, Carina

Knowledge-Based Reconstruction of Right Ventricular Volumes Using Real-time Three-dimensional Echocardiographic as Well as Cardiac Magnetic Resonance Images: Comparison With a Cardiac Magnetic Resonance Standard

JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY

IF6

2014-10-01

PREAI

Laser, Kai Thorsten; Horst, Jan-Pit; Barth, Peter; Kelter-Kloepping, Andrea; Haas, Nikolaus Alexander; Burchert, Wolfgang; Kececioglu, Deniz; Koerperich, Hermann

Impact of respiration on stroke volumes in paediatric controls and in patients after Fontan procedure assessed by MR real-time phase-velocity mapping

EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING

IF6.6

2014-09-21

OAAI

Koerperich, Hermann; Barth, Peter; Gieseke, Juergen; Mueller, Katja; Burchert, Wolfgang; Esdorn, Hermann; Kececioglu, Deniz; Beerbaum, Philipp; Laser, Kai Thorsten

EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations 脑桥小脑发育不全1型中的EXOSC3突变: 新突变和基因型-表型相关性

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2014-02-13

OAAI

Eggens, Veerle R. C.; Barth, Peter G.; Niermeijer, Jikke-Mien F.; Berg, Jonathan N.; Darin, Niklas; Dixit, Abhijit; Fluss, Joel; Foulds, Nicola; Fowler, Darren; Hortobagyi, Tibor; Jacques, Thomas; King, Mary D.; Makrythanasis, Periklis; Mate, Adrienn; Nicoll, James A. R.; O'Rourke, Declan; Price, Sue; Williams, Andrew N.; Wilson, Louise; Suri, Mohnish; Sztriha, Laszlo; Dijns-de Wissel, Marit B.; van Meegen, Mia T.; van Ruissen, Fred; Aronica, Eleonora; Troost, Dirk; Majoie, Charles B. L. M.; Marquering, Henk A.; Poll-The, Bwee Tien; Baas, Frank

Natural course of pontocerebellar hypoplasia type 2A

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2014-01-01

OAAI

Sanchez-Albisua, Iciar; Froelich, Saskia; Barth, Peter G.; Steinlin, Maja; Kraegeloh-Mann, Ingeborg

The neurology of rhizomelic chondrodysplasia punctata

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2013-10-30

OAAI

Bams-Mengerink, Annemieke M.; Koelman, Johannes H. T. M.; Waterham, Hans; Barth, Peter G.; Poll-The, Bwee Tien

Pontocerebellar hypoplasia type 1 Clinical spectrum and relevance of EXOSC3 mutations

NEUROLOGY

IF8.5

2013-01-29

OAAI

Rudnik-Schoeneborn, Sabine; Senderek, Jan; Jen, Joanna C.; Houge, Gunnar; Seeman, Pavel; Puchmajerova, Alena; Graul-Neumann, Luitgard; Seidel, Ulrich; Korinthenberg, Rudolf; Kirschner, Janbernd; Seeger, Juergen; Ryan, Monique M.; Muntoni, Francesco; Steinlin, Maja; Sztriha, Laszlo; Colomer, Jaume; Huebner, Christoph; Brockmann, Knut; Van Maldergem, Lionel; Schiff, Manuel; Holzinger, Andreas; Barth, Peter; Reardon, William; Yourshaw, Michael; Nelson, Stanley F.; Eggermann, Thomas; Zerres, Klaus

Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy

BRAIN

IF11.7

2013-01-28

OAAI

Weterman, Marian A. J.; Barth, Peter G.; van Spaendonck-Zwarts, Karin Y.; Aronica, Eleonora; Poll-The, Bwee-Tien; Brouwer, Oebele F.; van Tintelen, J. Peter; Qahar, Zohal; Bradley, Edward J.; de Wissel, Marit; Salviati, Leonardo; Angelini, Corrado; van den Heuvel, Lambertus; Thomasse, Yolande E. M.; Backx, Ad P.; Nurnberg, Gudrun; Nurnberg, Peter; Baas, Frank

Rhombencephalosynapsis: new findings in a larger study

BRAIN

IF11.7

2012-04-04

OAAI

Barth, Peter G.

Classification, diagnosis and potential mechanisms in Pontocerebellar Hypoplasia

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2011-07-12

134

OAAI

Namavar, Yasmin; Barth, Peter G.; Bwee Tien Poll-The; Baas, Frank

研究方向