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1.
J Phys Condens Matter ; 34(19)2022 Mar 09.
Article in English | MEDLINE | ID: mdl-35193132

ABSTRACT

We report on a microscopic study of the noncentrosymmetric superconductor W3Al2C (withTc= 7.6 K), mostly by means of27Al- and13C nuclear magnetic resonance (NMR). Since in this material the density of states at the Fermi level is dominated by the tungsten's 5dorbitals, we expect a sizeable spin-orbit coupling (SOC) effect. The normal-state electronic properties of W3Al2C resemble those of a standard metal, but with a Korringa product 1/(T1T) significantly smaller than that of metallic Al, reflecting the marginal role played bys-electrons. In the superconducting state, we observe a reduction of the Knight shift and an exponential decrease of the NMR relaxation rate 1/T1, typical ofs-wave superconductivity (SC). This is further supported by the observation of a small but distinct coherence peak just belowTcin the13C NMR relaxation-rate, in agreement with the fully-gapped superconducting state inferred from the electronic specific-heat data well belowTc. The above features are compared to those of members of the same family, in particular, Mo3Al2C, often claimed to exhibit unconventional SC. We discuss why, despite the enhanced SOC, W3Al2C does not show spin-triplet features in its superconducting state and consider the broader consequences of our results for noncentrosymmetric superconductors in general.

3.
Clin Exp Dermatol ; 46(3): 462-472, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33207021

ABSTRACT

The current COVID-19 pandemic is caused by the SARS-CoV-2 coronavirus. The initial recognized symptoms were respiratory, sometimes culminating in severe respiratory distress requiring ventilation, and causing death in a percentage of those infected. As time has passed, other symptoms have been recognized. The initial reports of cutaneous manifestations were from Italian dermatologists, probably because Italy was the first European country to be heavily affected by the pandemic. The overall clinical presentation, course and outcome of SARS-CoV-2 infection in children differ from those in adults as do the cutaneous manifestations of childhood. In this review, we summarize the current knowledge on the cutaneous manifestations of COVID-19 in children after thorough and critical review of articles published in the literature and from the personal experience of a large panel of paediatric dermatologists in Europe. In Part 1, we discuss one of the first and most widespread cutaneous manifestations of COVID-19, chilblain-like lesions, and in Part 2 we expanded to other manifestations, including erythema multiforme, urticaria and Kawasaki disease-like inflammatory multisystemic syndrome. In this part of the review, we discuss the histological findings of COVID-19 manifestations, and the testing and management of infected children for both COVID-19 and any other pre-existing conditions.


Subject(s)
COVID-19/complications , Skin Diseases, Viral/pathology , Adolescent , Antibodies, Monoclonal, Humanized/therapeutic use , COVID-19/diagnosis , COVID-19/pathology , COVID-19 Testing , Child , Dermatologic Agents/therapeutic use , Exanthema/drug therapy , Exanthema/pathology , Exanthema/virology , Humans , Nicolau Syndrome/drug therapy , Nicolau Syndrome/pathology , Nicolau Syndrome/virology , Pityriasis Rosea/pathology , Pityriasis Rosea/virology , Purpura/drug therapy , Purpura/pathology , Purpura/virology , SARS-CoV-2 , Skin Diseases, Viral/drug therapy , Urticaria/drug therapy , Urticaria/pathology , Urticaria/virology
4.
Clin Exp Dermatol ; 46(3): 451-461, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33166429

ABSTRACT

The current COVID-19 pandemic is caused by the SARS-CoV-2 coronavirus. The initial recognized symptoms were respiratory, sometimes culminating in severe respiratory distress requiring ventilation, and causing death in a percentage of those infected. As time has passed, other symptoms have been recognized. The initial reports of cutaneous manifestations were from Italian dermatologists, probably because Italy was the first European country to be heavily affected by the pandemic. The overall clinical presentation, course and outcome of SARS-CoV-2 infection in children differ from those in adults, as do the cutaneous manifestations of childhood. In this review, we summarize the current knowledge on the cutaneous manifestations of COVID-19 in children after thorough and critical review of articles published in the literature and from the personal experience of a large panel of paediatric dermatologists in Europe. In Part 1, we discussed one of the first and most widespread cutaneous manifestations of COVID-19, chilblain-like lesions. In this part of the review, we describe other manifestations, including erythema multiforme, urticaria and Kawasaki disease-like inflammatory multisystemic syndrome. In Part 3, we discuss the histological findings of COVID-19 manifestations, and the testing and management of infected children for both COVID-19 and any other pre-existing conditions.


Subject(s)
COVID-19/complications , Erythema Multiforme/virology , Mucocutaneous Lymph Node Syndrome/virology , Urticaria/virology , Adolescent , COVID-19/pathology , Child , Erythema Multiforme/pathology , Exanthema/pathology , Exanthema/virology , Humans , SARS-CoV-2 , Urticaria/pathology
5.
Clin Exp Dermatol ; 46(3): 444-450, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33180982

ABSTRACT

The current COVID-19 pandemic is caused by the SARS-CoV-2 coronavirus. The initial recognized symptoms were respiratory, sometimes culminating in severe respiratory distress requiring ventilation, and causing death in a percentage of those infected. As time has passed, other symptoms have been recognized. The initial reports of cutaneous manifestations were from Italian dermatologists, probably because Italy was the first European country to be heavily affected by the pandemic. The overall clinical presentation, course and outcome of SARS-CoV-2 infection in children differ from those in adults as do the cutaneous manifestations of childhood. In this review, we summarize the current knowledge on the cutaneous manifestations of COVID-19 in children after thorough and critical review of articles published in the literature and from the personal experience of a large panel of paediatric dermatologists in Europe. In Part 1, we discuss one of the first and most widespread cutaneous manifestation of COVID-19, chilblain-like lesions. In Part 2, we review other manifestations, including erythema multiforme, urticaria and Kawasaki disease-like inflammatory multisystemic syndrome, while in Part 3, we discuss the histological findings of COVID-19 manifestations, and the testing and management of infected children, for both COVID-19 and any other pre-existing conditions.


Subject(s)
COVID-19/complications , Chilblains/virology , Adolescent , COVID-19/diagnosis , COVID-19/pathology , COVID-19/therapy , COVID-19 Testing , Chilblains/immunology , Chilblains/pathology , Child , Humans , Interferon Type I/immunology , Remission, Spontaneous , Risk Factors , SARS-CoV-2 , Thrombosis/etiology , Vasculitis/etiology
6.
BMC Musculoskelet Disord ; 21(1): 844, 2020 Dec 18.
Article in English | MEDLINE | ID: mdl-33339540

ABSTRACT

PURPOSE: Reconstruction of the Anterior cruciate ligament (ACL) using tendon grafting is an established method for restoring knee function and stability. Multiple methods are established for graft fixation. Several involve anchoring the autograft distant to the joint with hardware that remains implanted. This study reports the first early to midterm results in patients who received ACL reconstruction (ACLR) using the T-Lock Osteotrans femoral near joint fixation method with a tibial fixation using the BioactIF Osteotrans interference screw. METHODS: This consecutive prospective series included 20 Patients (14 Male, 6 Female) with a primary ACL rupture. All patients were treated with an ACLR using a semitendinosus autograft fixated with the T-Lock Osteotrans and were followed-up postoperatively. The following parameters were assessed: Side-to-side difference of the posterior-anterior translation measured using the KT-1000 arthrometer, Tegner activity score, Lysholm score, IKDC subjective knee evaluation form. Magnetic resonance imaging (MRI) was done to assess tunnel enlargement and integrity of the anchoring device. RESULTS: The average follow-up duration was 2 years (range 1-4.2 years). One patient was lost to follow-up. Two Patients suffered a traumatic ACL re-rupture 2 years postoperatively and received a 2-stage revision ACLR. Difference in the posterior-anterior translation was 1.8 mm (range 0-5). The median Tegner score was 6 (range 4-10) and 9 patients (45%) returned to their preinjury level of activity. The mean IKDC subjective knee evaluation form scored 91 points (range 77-100). The mean Lysholm score was 86 points (74-96). All mentioned scores were significantly better compared to preoperative values. No relevant tunnel enlargement was seen on MRI. The anchoring device was evaluated to be intact in all patients. CONCLUSION: ACLR with the aforementioned procedure leads to good clinical and radiological outcome.


Subject(s)
Anterior Cruciate Ligament Injuries , Anterior Cruciate Ligament Reconstruction , Adolescent , Adult , Anterior Cruciate Ligament Injuries/diagnostic imaging , Anterior Cruciate Ligament Injuries/surgery , Female , Follow-Up Studies , Humans , Knee Joint/diagnostic imaging , Knee Joint/surgery , Male , Prospective Studies , Tendons/diagnostic imaging , Tendons/surgery , Treatment Outcome , Young Adult
8.
Rev Sci Instrum ; 90(1): 013901, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30709234

ABSTRACT

The investigation of materials under extreme pressure conditions requires high-performance cells whose design invariably involves trade-offs between the maximum achievable pressure, the allowed sample volume, and the possibility of real-time pressure monitoring. With a newly conceived hybrid piston-clamped anvil cell, we offer a relatively simple and versatile system, suitable for nuclear magnetic resonance experiments up to 4.4 GPa. Finite-element models, taking into account mechanical and thermal conditions, were used to optimize and validate the design prior to the realization of the device. Cell body and gaskets were made of beryllium-copper alloy and the pistons and pusher were made of tungsten carbide, while the anvils consist of zirconium dioxide. The low-temperature pressure cell performance was tested by monitoring in situ the pressure-dependent 63Cu nuclear-quadrupole-resonance signal of Cu2O.

9.
Br J Dermatol ; 180(3): 484-495, 2019 03.
Article in English | MEDLINE | ID: mdl-29897631

ABSTRACT

These guidelines for the management of congenital ichthyoses have been developed by a multidisciplinary group of European experts following a systematic review of the current literature, an expert conference held in Toulouse in 2016, and a consensus on the discussions. These guidelines summarize evidence and expert-based recommendations and intend to help clinicians with the management of these rare and often complex diseases. These guidelines comprise two sections. This is part two, covering the management of complications and the particularities of some forms of congenital ichthyosis.


Subject(s)
Consensus , Dermatology/standards , Ichthyosiform Erythroderma, Congenital/therapy , Ichthyosis/therapy , Infant, Premature, Diseases/therapy , Dermatology/methods , Europe , Humans , Ichthyosiform Erythroderma, Congenital/complications , Ichthyosis/complications
10.
Br J Dermatol ; 180(2): 272-281, 2019 02.
Article in English | MEDLINE | ID: mdl-30216406

ABSTRACT

These guidelines for the management of congenital ichthyoses have been developed by a multidisciplinary group of European experts following a systematic review of the current literature, an expert conference held in Toulouse in 2016 and a consensus on the discussions. They summarize evidence and expert-based recommendations and are intended to help clinicians with the management of these rare and often complex diseases. These guidelines comprise two sections. This is part one, covering topical therapies, systemic therapies, psychosocial management, communicating the diagnosis and genetic counselling.


Subject(s)
Behavior Therapy/standards , Consensus , Dermatologic Agents/therapeutic use , Dermatology/standards , Ichthyosiform Erythroderma, Congenital/therapy , Administration, Oral , Administration, Topical , Behavior Therapy/methods , Dermatology/methods , Europe , Genetic Counseling/standards , Humans , Ichthyosiform Erythroderma, Congenital/diagnosis , Ichthyosiform Erythroderma, Congenital/psychology , Quality of Life , Social Support , Systematic Reviews as Topic
11.
Radiologe ; 59(3): 198-203, 2019 Mar.
Article in German | MEDLINE | ID: mdl-30367224

ABSTRACT

BACKGROUND: Especially in sports like professional football (soccer) making a diagnosis and generating a final prognosis concerning the time loss is demanding for the team physician and the radiologist. Therefore, the radiologist has to fulfill the requests concerning availability and quality of imaging. This is a particularly difficult task for groin pain because it can be caused by a variety of pathologies. OBJECTIVES: In addition to the question what the sports physician expects from the radiologist, we have to look at which information the radiologist needs to answer the raised questions. Which external circumstances make a change of the normal procedures necessary when supporting athletes? RESULTS AND DISCUSSION: Close collaboration between the radiologist and sports physician guarantees that the raised questions from the athlete and the club concerning time loss and necessary therapy can be answered. Thus, the sports physician has to give the radiologist detailed information regarding symptoms, location of the pain and other clinical findings. The radiologist has to include this information into the interpretation of the images to distinguish safely between findings caused by the actual injury and those which are pre-existing.


Subject(s)
Athletic Injuries , Sports , Athletes , Groin/physiology , Humans , Pain , Radiologists
12.
Nat Commun ; 9(1): 2238, 2018 06 08.
Article in English | MEDLINE | ID: mdl-29884824

ABSTRACT

Feshbach resonances are a powerful tool to tune the interaction in an ultracold atomic gas. The commonly used magnetic Feshbach resonances are specific for each species and are restricted with respect to their temporal and spatial modulation. Optical Feshbach resonances are an alternative which can overcome this limitation. Here, we show that ultra-long-range Rydberg molecules can be used to implement an optical Feshbach resonance. Tuning the on-site interaction of a degenerate Bose gas in a 3D optical lattice, we demonstrate a similar performance compared to recent realizations of optical Feshbach resonances using intercombination transitions. Our results open up a class of optical Feshbach resonances with a plenitude of available lines for many atomic species and the possibility to further increase the performance by carefully selecting the underlying Rydberg state.

15.
Hautarzt ; 68(10): 796-802, 2017 Oct.
Article in German | MEDLINE | ID: mdl-28871316

ABSTRACT

Neonatal, ichthyosiform erythroderma is rare and may be associated with primarily cutaneous disorders as well as with a broad spectrum of potentially severe underlying diseases. Neonatal erythroderma represents a pediatric dermatological emergency requiring a swift diagnosis and effective, interdisciplinary management. This review summarizes both primary skin diseases and systemic illnesses that are known to elicit erythroderma in neonates and young infants.


Subject(s)
Emergencies , Ichthyosiform Erythroderma, Congenital/diagnosis , Comorbidity , Diagnosis, Differential , Early Diagnosis , Early Medical Intervention , Humans , Ichthyosiform Erythroderma, Congenital/therapy , Infant , Infant, Newborn , Interdisciplinary Communication , Intersectoral Collaboration
16.
Hautarzt ; 68(10): 772-773, 2017 Oct.
Article in German | MEDLINE | ID: mdl-28879454
17.
Nat Commun ; 8(1): 156, 2017 07 31.
Article in English | MEDLINE | ID: mdl-28761126

ABSTRACT

Unlike the widely studied ReFeAsO series, the newly discovered iron-based superconductor ThFeAsN exhibits a remarkably high critical temperature of 30 K, without chemical doping or external pressure. Here we investigate in detail its magnetic and superconducting properties via muon-spin rotation/relaxation and nuclear magnetic resonance techniques and show that ThFeAsN exhibits strong magnetic fluctuations, suppressed below ~35 K, but no magnetic order. This contrasts strongly with the ReFeAsO series, where stoichiometric parent materials order antiferromagnetically and superconductivity appears only upon doping. The ThFeAsN case indicates that Fermi-surface modifications due to structural distortions and correlation effects are as important as doping in inducing superconductivity. The direct competition between antiferromagnetism and superconductivity, which in ThFeAsN (as in LiFeAs) occurs at already zero doping, may indicate a significant deviation of the s-wave superconducting gap in this compound from the standard s ± scenario.Exploring the interplay between the superconducting gap and the antiferromagnetic phase in Fe-based superconductors remains an open issue. Here, the authors show that Fermi-surface modifications by means of structural distortions and correlation effects are as important as doping in inducing superconductivity in undoped ThFeAsN.

18.
Hautarzt ; 68(7): 571-582, 2017 Jul.
Article in German | MEDLINE | ID: mdl-28474101

ABSTRACT

Chronic urticaria (CU) is defined by episodes of urticaria with or without angioedema, which recur daily or nearly daily over more than 6 weeks. Sudden manifestations of CU with or without known causes are termed chronic spontaneous urticaria, which is differentiated from chronic inducible urticaria. The differential diagnoses of CU in childhood range from self-limiting dermatoses to severe systemic diseases. Further targeted steps are taken to detect potential trigger factors or underlying illnesses only if suspicion arises on anamnestic grounds and CU is best treated in accordance with international guidelines. First-line therapy consists of non-sedating H1-antihistamines at approved or even higher doses. If symptoms persist, additional treatment with omalizumab, cyclosporine or montelukast can be initiated after careful individual consideration.


Subject(s)
Urticaria/diagnosis , Acetates/therapeutic use , Angioedema/diagnosis , Angioedema/drug therapy , Angioedema/etiology , Angioedema/pathology , Child , Child, Preschool , Chronic Disease , Cyclopropanes , Cyclosporine/therapeutic use , Diagnosis, Differential , Guideline Adherence , Histamine Antagonists/therapeutic use , Humans , Infant , Long-Term Care , Omalizumab/therapeutic use , Quinolines/therapeutic use , Skin/pathology , Sulfides , Urticaria/drug therapy , Urticaria/etiology , Urticaria/pathology
20.
Hautarzt ; 67(4): 279-86, 2016 Apr.
Article in German | MEDLINE | ID: mdl-26943360

ABSTRACT

Hereditary epidermolysis bullosa (EB) represents a clinically heterogeneous group of congenital blistering disorders requiring multiprofessional care. EB is associated with a broad spectrum of potentially severe complications often reaching their full extent during school age and adolescence. This review aims at summarizing cutaneous manifestations of EB as well as extracutaneous complications of this complex disease and their interdisciplinary management.


Subject(s)
Epidermolysis Bullosa/diagnosis , Epidermolysis Bullosa/therapy , Patient Care Team/organization & administration , Adolescent , Adolescent Health/trends , Child , Child Health/trends , Child, Preschool , Dermatology/trends , Early Diagnosis , Epidermolysis Bullosa/psychology , Female , Germany , Humans , Infant , Infant, Newborn , Male , Patient Care Management/organization & administration , Psychology, Adolescent/trends , Psychology, Child/trends , Young Adult
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